7464-56-4,MFCD04973540
Catalog No.:AA005IZ6

7464-56-4 | Allyl alpha-d-glucopyranoside

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
97%
in stock  
$96.00   $68.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA005IZ6
Chemical Name:
Allyl alpha-d-glucopyranoside
CAS Number:
7464-56-4
Molecular Formula:
C9H16O6
Molecular Weight:
220.2197
MDL Number:
MFCD04973540
SMILES:
C=CCO[C@H]1O[C@H](CO)[C@H]([C@@H]([C@H]1O)O)O
Properties
Properties
 
BP:
415?°C at 760 mmHg  
Form:
Solid  
MP:
138-141°C  
Storage:
Keep in dry area;2-8℃;  

Computed Properties
 
Complexity:
209  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
5  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
15  
Hydrogen Bond Acceptor Count:
6  
Hydrogen Bond Donor Count:
4  
Isotope Atom Count:
0  
Rotatable Bond Count:
4  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
-1.6  

Downstream Synthesis Route

[1]Locationinpatent:schemeortableHassan,HammedH.A.M.[LettersinOrganicChemistry,2010,vol.7,#2,p.127-135]

[2]Talleyetal.[JournaloftheAmericanChemicalSociety,1945,vol.67,p.2037]Daniellietal.[BiochemicalJournal,1947,vol.41,p.325,332]

[3]Hetfleisch-Stephan;Schunk;Rudiger[Pharmazie,1994,vol.49,#2-3,p.125-130]

[4]Koto,Shinkiti;Shinoda,Yoshika;Hirooka,Motoko;Sekino,Akiko;Ishizumi,Sachiko;Koma,Mutsuko;Matuura,Chieko;Sakata,Naoko[BulletinoftheChemicalSocietyofJapan,2003,vol.76,#8,p.1603-1615]

[1]Locationinpatent:experimentalpartHassan,HammedH.A.M.[LettersinOrganicChemistry,2010,vol.7,#2,p.127-135]

[2]Talleyetal.[JournaloftheAmericanChemicalSociety,1945,vol.67,p.2037]

[1]Schindler,CorinnaS.;Bertschi,Louis;Carreira,ErickM.[AngewandteChemie-InternationalEdition,2010,vol.49,#48,p.9229-9232]

[2]Wang,Yanhui;Zhao,Xiaoke;Kong,Qiuyun;Yao,Jiajian;Meng,Xiangbao;Li,Zhongjun[TetrahedronLetters,2017,vol.58,#16,p.1655-1658]

[3]Locationinpatent:experimentalpartTursky,Matyas;Vesely,Jan;Tislerova,Iva;Trnka,Tomas;Ledvina,Miroslav[Synthesis,2008,#16,p.2610-2616]

[4]Pelyvas,Istvan;Lindhorst,Thisbe;Thiem,Joachim[LiebigsAnnalenderChemie,1990,#8,p.761-769]

[5]Holme,KevinR.;Hall,LauranceD.[CarbohydrateResearch,1992,vol.225,#2,p.291-306]

[6]Nepogod'ev,SergeyA.;Backinowsky,LeonV.;Grzeszczyk,Barbara;Zamojski,Aleksander[CarbohydrateResearch,1994,vol.254,p.43-60]

[7]Wolfenden,MarkL.;Cloninger,MaryJ.[JournaloftheAmericanChemicalSociety,2005,vol.127,#35,p.12168-12169]

[8]CurrentPatentAssignee:OTSUKAHOLDINGSCOLTD-WO2011/137181,2011,A1Locationinpatent:Page/Pagecolumn36

[9]Koch,Stefan;Schollmeyer,Dieter;Löwe,Holger;Kunz,Horst[Chemistry-AEuropeanJournal,2013,vol.19,#22,p.7020-7041]

[10]Tsai,Charng-Sheng;Chen,Chao-Tsen[CollectionofCzechoslovakChemicalCommunications,2012,vol.77,#4,p.314-322]

[11]Ruike,Tatsushi;Kanai,Yoshihiro;Iwabata,Kazuki;Matsumoto,Yuki;Murata,Hiroshi;Ishima,Masahiro;Ohta,Keisuke;Oshige,Masahiko;Katsura,Shinji;Kuramochi,Koji;Kamisuki,Shinji;Sahara,Hiroeki;Miura,Masahiko;Sugawara,Fumio;Sakaguchi,Kengo[Xenobiotica,2018,p.1-17]

2280-44-6    107-18-6   
allylβ-D-glucopyranoside 
  7464-56-4 

[1]Jenkins,DavidJ.;Potter,BarryV.L.[CarbohydrateResearch,1996,vol.287,#2,p.169-182]

[2]Konradsson,Peter;Roberts,Carmichael;Fraser-Reid,Bert[RecueildesTravauxChimiquesdesPays-Bas,1991,vol.110,#1,p.23-24]

[3]Jenkins;Potter[JournaloftheChemicalSociety.Chemicalcommunications,1995,#11,p.1169-1170]

[4]Nepogod'ev,SergeyA.;Backinowsky,LeonV.;Grzeszczyk,Barbara;Zamojski,Aleksander[CarbohydrateResearch,1994,vol.254,p.43-60]

[5]Jenkins;Potter[JournaloftheChemicalSociety.Chemicalcommunications,1995,#11,p.1169-1170]

[6]Fang,TammyT.;Bendiak,Brad[JournaloftheAmericanChemicalSociety,2007,vol.129,#31,p.9721-9736]

[7]Locationinpatent:experimentalpartJavierMunoz;Andre,Sabine;Gabius,Hans-Joachin;Sinisterra,JoseV.;Hernaiz,MariaJ.;Linhardt,RobertJ.[GreenChemistry,2009,vol.11,#3,p.373-379]

[8]Locationinpatent:schemeortableAuge,Jacques;Sizun,Gwenaelle[GreenChemistry,2009,vol.11,#8,p.1179-1183]

[9]Gorityala,BalaKishan;Ma,Jimei;Pasunooti,KalyanKumar;Cai,Shuting;Liu,Xue-Wei[GreenChemistry,2011,vol.13,#3,p.573-577]

[10]Silverberg,LeeJ.;Dillon,JohnL.;Vemishetti,Purushotham;Sleezer,PaulD.;Discordia,RobertP.;Hartung,KerryB.;Gao,Qi[OrganicProcessResearchandDevelopment,2000,vol.4,#1,p.34-42]

[1]Ziegler;Eckhardt;Neumann;Birault[Synthesis,1992,#10,p.1013-1017]

[2]Oltvoort,J.J.;Boeckel,C.A.A.van;Koning,J.H.de;Boom,J.H.van[Synthesis,1981,#4,p.305-308]

Literature

Title: Comparison of two kinds of nanomedicine for targeted gene therapy: premodified or postmodified gene delivery systems.

Journal: International journal of nanomedicine 20120101

Title: Agglutination study of poly(allyl-alpha-D-glucopyranose/styrene) latex particles in the presence of Concanavalin A.

Journal: Colloids and surfaces. B, Biointerfaces 20050325

Title: Determination of etoposide phosphate intermediates by gradient liquid chromatography using postcolumn derivatization with cuprammonium hydroxide.

Journal: Journal of chromatography. A 20020405

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Additional Info:
SDS
Tags:7464-56-4 Molecular Formula|7464-56-4 MDL|7464-56-4 SMILES|7464-56-4 Allyl alpha-d-glucopyranoside
Catalog No.: AA005IZ6
7464-56-4,MFCD04973540
7464-56-4 | Allyl alpha-d-glucopyranoside
Pack Size: 250mg
Purity: 97%
in stock
$96.00 $68.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA005IZ6
Chemical Name: Allyl alpha-d-glucopyranoside
CAS Number: 7464-56-4
Molecular Formula: C9H16O6
Molecular Weight: 220.2197
MDL Number: MFCD04973540
SMILES: C=CCO[C@H]1O[C@H](CO)[C@H]([C@@H]([C@H]1O)O)O
Properties
BP: 415?°C at 760 mmHg  
Form: Solid  
MP: 138-141°C  
Storage: Keep in dry area;2-8℃;  
Complexity: 209  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 5  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 15  
Hydrogen Bond Acceptor Count: 6  
Hydrogen Bond Donor Count: 4  
Isotope Atom Count: 0  
Rotatable Bond Count: 4  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: -1.6  
Downstream Synthesis Route
50-99-7    107-18-6    7464-56-4 

[1]Locationinpatent:schemeortableHassan,HammedH.A.M.[LettersinOrganicChemistry,2010,vol.7,#2,p.127-135]

[2]Talleyetal.[JournaloftheAmericanChemicalSociety,1945,vol.67,p.2037]Daniellietal.[BiochemicalJournal,1947,vol.41,p.325,332]

[3]Hetfleisch-Stephan;Schunk;Rudiger[Pharmazie,1994,vol.49,#2-3,p.125-130]

[4]Koto,Shinkiti;Shinoda,Yoshika;Hirooka,Motoko;Sekino,Akiko;Ishizumi,Sachiko;Koma,Mutsuko;Matuura,Chieko;Sakata,Naoko[BulletinoftheChemicalSocietyofJapan,2003,vol.76,#8,p.1603-1615]

106-95-6    7464-56-4    185564-68-5 

[1]Locationinpatent:experimentalpartHassan,HammedH.A.M.[LettersinOrganicChemistry,2010,vol.7,#2,p.127-135]

[2]Talleyetal.[JournaloftheAmericanChemicalSociety,1945,vol.67,p.2037]

2280-44-6    107-18-6    7464-56-4 

[1]Schindler,CorinnaS.;Bertschi,Louis;Carreira,ErickM.[AngewandteChemie-InternationalEdition,2010,vol.49,#48,p.9229-9232]

[2]Wang,Yanhui;Zhao,Xiaoke;Kong,Qiuyun;Yao,Jiajian;Meng,Xiangbao;Li,Zhongjun[TetrahedronLetters,2017,vol.58,#16,p.1655-1658]

[3]Locationinpatent:experimentalpartTursky,Matyas;Vesely,Jan;Tislerova,Iva;Trnka,Tomas;Ledvina,Miroslav[Synthesis,2008,#16,p.2610-2616]

[4]Pelyvas,Istvan;Lindhorst,Thisbe;Thiem,Joachim[LiebigsAnnalenderChemie,1990,#8,p.761-769]

[5]Holme,KevinR.;Hall,LauranceD.[CarbohydrateResearch,1992,vol.225,#2,p.291-306]

[6]Nepogod'ev,SergeyA.;Backinowsky,LeonV.;Grzeszczyk,Barbara;Zamojski,Aleksander[CarbohydrateResearch,1994,vol.254,p.43-60]

[7]Wolfenden,MarkL.;Cloninger,MaryJ.[JournaloftheAmericanChemicalSociety,2005,vol.127,#35,p.12168-12169]

[8]CurrentPatentAssignee:OTSUKAHOLDINGSCOLTD-WO2011/137181,2011,A1Locationinpatent:Page/Pagecolumn36

[9]Koch,Stefan;Schollmeyer,Dieter;Löwe,Holger;Kunz,Horst[Chemistry-AEuropeanJournal,2013,vol.19,#22,p.7020-7041]

[10]Tsai,Charng-Sheng;Chen,Chao-Tsen[CollectionofCzechoslovakChemicalCommunications,2012,vol.77,#4,p.314-322]

[11]Ruike,Tatsushi;Kanai,Yoshihiro;Iwabata,Kazuki;Matsumoto,Yuki;Murata,Hiroshi;Ishima,Masahiro;Ohta,Keisuke;Oshige,Masahiko;Katsura,Shinji;Kuramochi,Koji;Kamisuki,Shinji;Sahara,Hiroeki;Miura,Masahiko;Sugawara,Fumio;Sakaguchi,Kengo[Xenobiotica,2018,p.1-17]

2280-44-6    107-18-6   
allylβ-D-glucopyranoside 
  7464-56-4 

[1]Jenkins,DavidJ.;Potter,BarryV.L.[CarbohydrateResearch,1996,vol.287,#2,p.169-182]

[2]Konradsson,Peter;Roberts,Carmichael;Fraser-Reid,Bert[RecueildesTravauxChimiquesdesPays-Bas,1991,vol.110,#1,p.23-24]

[3]Jenkins;Potter[JournaloftheChemicalSociety.Chemicalcommunications,1995,#11,p.1169-1170]

[4]Nepogod'ev,SergeyA.;Backinowsky,LeonV.;Grzeszczyk,Barbara;Zamojski,Aleksander[CarbohydrateResearch,1994,vol.254,p.43-60]

[5]Jenkins;Potter[JournaloftheChemicalSociety.Chemicalcommunications,1995,#11,p.1169-1170]

[6]Fang,TammyT.;Bendiak,Brad[JournaloftheAmericanChemicalSociety,2007,vol.129,#31,p.9721-9736]

[7]Locationinpatent:experimentalpartJavierMunoz;Andre,Sabine;Gabius,Hans-Joachin;Sinisterra,JoseV.;Hernaiz,MariaJ.;Linhardt,RobertJ.[GreenChemistry,2009,vol.11,#3,p.373-379]

[8]Locationinpatent:schemeortableAuge,Jacques;Sizun,Gwenaelle[GreenChemistry,2009,vol.11,#8,p.1179-1183]

[9]Gorityala,BalaKishan;Ma,Jimei;Pasunooti,KalyanKumar;Cai,Shuting;Liu,Xue-Wei[GreenChemistry,2011,vol.13,#3,p.573-577]

[10]Silverberg,LeeJ.;Dillon,JohnL.;Vemishetti,Purushotham;Sleezer,PaulD.;Discordia,RobertP.;Hartung,KerryB.;Gao,Qi[OrganicProcessResearchandDevelopment,2000,vol.4,#1,p.34-42]

69304-37-6    7464-56-4    78120-20-4 

[1]Ziegler;Eckhardt;Neumann;Birault[Synthesis,1992,#10,p.1013-1017]

[2]Oltvoort,J.J.;Boeckel,C.A.A.van;Koning,J.H.de;Boom,J.H.van[Synthesis,1981,#4,p.305-308]

Literature fold

Title: Comparison of two kinds of nanomedicine for targeted gene therapy: premodified or postmodified gene delivery systems.

Journal: International journal of nanomedicine20120101

Title: Agglutination study of poly(allyl-alpha-D-glucopyranose/styrene) latex particles in the presence of Concanavalin A.

Journal: Colloids and surfaces. B, Biointerfaces20050325

Title: Determination of etoposide phosphate intermediates by gradient liquid chromatography using postcolumn derivatization with cuprammonium hydroxide.

Journal: Journal of chromatography. A20020405

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