+1 858-523-8231
Login | Register
menu
AA Blocks, Building Blocks, Catalysts, Inhibitors
Login | Register
673-32-5,MFCD05864082
Catalog No.:AA00FA8G

673-32-5 | 1-Phenyl-1-propyne

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
95%
in stock  
$36.00   $25.00
- +
1g
95%
in stock  
$50.00   $35.00
- +
5g
>98%
in stock  
$100.00   $70.00
- +
10g
>98%
in stock  
$163.00   $114.00
- +
25g
>98%
in stock  
$306.00   $214.00
- +
100g
>98%
in stock  
$941.00   $659.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA00FA8G
Chemical Name:
1-Phenyl-1-propyne
CAS Number:
673-32-5
Molecular Formula:
C9H8
Molecular Weight:
116.1598
MDL Number:
MFCD05864082
SMILES:
CC#CC1=CC=CC=C1
Properties
Properties
 
BP:
182°C at 760 mmHg  
Form:
Liquid  
Refractive Index:
n20/D 1.564(lit.)  
Storage:
Inert atmosphere;2-8℃;  

Computed Properties
 
Complexity:
127  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
0  
Hydrogen Bond Donor Count:
0  
Isotope Atom Count:
0  
Rotatable Bond Count:
1  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
3  

Upstream Synthesis Route

[1]Patent:CN105859647,2016,A,.Locationinpatent:Paragraph0027;0028;0029

[2]Patent:CN105418528,2016,A,.Locationinpatent:Paragraph0061;0062

[1]JournaloftheAmericanChemicalSociety,1989,vol.111,#16,p.6008-6014

[1]JournaloftheAmericanChemicalSociety,1989,vol.111,#16,p.6008-6014

[1]HelveticaChimicaActa,2016,vol.99,#9,p.665-673

[1]HelveticaChimicaActa,2016,vol.99,#9,p.665-673

Downstream Synthesis Route

[1]TetrahedronLetters,1998,vol.39,p.627-630

673-32-5    31930-34-4   
ethyl2-(2',4'-diphenyl-3',5'-dimethyl-1'-cyclopentadienyl)ethanoate 

[1]Tetrahedron,1999,vol.55,p.4969-4978

110-86-1    673-32-5   
ammoniumhydroxide 
 
sulfur 
  102-93-2 

[1]JournaloftheAmericanChemicalSociety,1946,vol.68,p.2029,2032,2755

[1]JournalofOrganicChemistry,2000,vol.65,p.2287-2291

673-32-5    4464-18-0   
1,3,5-Tris-((E)-3-phenyl-allyloxymethyl)-benzene 

[1]TetrahedronLetters,2001,vol.42,p.6207-6210

Literature

Title: Phenylpropargyl radicals and their dimerization products: an IR/UV double resonance study.

Journal: The journal of physical chemistry. A 20120823

Title: Ab initio/RRKM-ME study on the mechanism and kinetics of the reaction of phenyl radical with 1,2-butadiene.

Journal: The journal of physical chemistry. A 20100729

Title: Photoionization of three isomers of the C9H7 radical.

Journal: The journal of physical chemistry. A 20100415

Title: Reaction dynamics of phenyl radicals in extreme environments: a crossed molecular beam study.

Journal: Accounts of chemical research 20090217

Title: Cross-coupling reaction of alkyl halides with grignard reagents catalyzed by Ni, Pd, or Cu complexes with pi-carbon ligand(s).

Journal: Accounts of chemical research 20081118

Title: 1-Phenyl-1-propyne on Cu(111): TOFMS TPD, XPS, UPS, and 2PPE Studies.

Journal: Langmuir : the ACS journal of surfaces and colloids 20071120

Title: Copper-catalyzed cross-coupling reaction of grignard reagents with primary-alkyl halides: remarkable effect of 1-phenylpropyne.

Journal: Angewandte Chemie (International ed. in English) 20070101

Title: Reactivity of alkynes containing alpha-hydrogen atoms with a triruthenium hydrido carbonyl cluster: alkenyl versus allyl cluster derivatives.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany) 20051007

Title: [Ind(2)TiMe(2)]: a general catalyst for the intermolecular hydroamination of alkynes.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany) 20040621

Title: Regiochemical variation in the electrophilic addition of HBr to 1-phenylprop-1-yne.

Journal: Organic & biomolecular chemistry 20030621

Title: The concerted addition of HBr to aryl alkynes; orthogonal pi bond selectivity.

Journal: Organic & biomolecular chemistry 20030621

Title: Cp*(2)TiMe(2): an improved catalyst for the intermolecular addition of n-alkyl- and benzylamines to alkynes.

Journal: The Journal of organic chemistry 20020322

Quotation Request
Company Name:
*
Contact Person:
*
Email:
*
Quantity Required:
*
Country:
Additional Info:
Submit
SDS
Related Products of 673-32-5
Building Blocks
More >
Historical Records
174219-86-4

174219-86-4

 436155-36-1

436155-36-1

 1038374-82-1

1038374-82-1

 2503-39-1

2503-39-1

 341009-06-1

341009-06-1

 390-16-9

390-16-9
Tags:673-32-5 Molecular Formula|673-32-5 MDL|673-32-5 SMILES|673-32-5 1-Phenyl-1-propyne
Catalog No.: AA00FA8G
673-32-5,MFCD05864082
673-32-5 | 1-Phenyl-1-propyne
Pack Size： 250mg
Purity： 95%
in stock
$36.00 $25.00
Pack Size： 1g
Purity： 95%
in stock
$50.00 $35.00
Pack Size： 5g
Purity： >98%
in stock
$100.00 $70.00
Pack Size： 10g
Purity： >98%
in stock
$163.00 $114.00
Pack Size： 25g
Purity： >98%
in stock
$306.00 $214.00
Pack Size： 100g
Purity： >98%
in stock
$941.00 $659.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA00FA8G
Chemical Name: 1-Phenyl-1-propyne
CAS Number: 673-32-5
Molecular Formula: C9H8
Molecular Weight: 116.1598
MDL Number: MFCD05864082
SMILES: CC#CC1=CC=CC=C1
Properties
BP: 182°C at 760 mmHg  
Form: Liquid  
Refractive Index: n20/D 1.564(lit.)  
Storage: Inert atmosphere;2-8℃;  
Complexity: 127  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 9  
Hydrogen Bond Acceptor Count: 0  
Hydrogen Bond Donor Count: 0  
Isotope Atom Count: 0  
Rotatable Bond Count: 1  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 3  
Upstream Synthesis Route
673-32-5    932-90-1    37928-17-9 

[1]Patent:CN105859647,2016,A,.Locationinpatent:Paragraph0027;0028;0029

[2]Patent:CN105418528,2016,A,.Locationinpatent:Paragraph0061;0062

593-53-3    536-74-3    673-32-5    766-47-2    766-82-5    766-97-2 

[1]JournaloftheAmericanChemicalSociety,1989,vol.111,#16,p.6008-6014

67-56-1    593-53-3    536-74-3    673-32-5    766-47-2    766-82-5    577-16-2    766-97-2 

[1]JournaloftheAmericanChemicalSociety,1989,vol.111,#16,p.6008-6014

673-32-5    124-38-9    625-81-0    1199-77-5    1643935-57-2 

[1]HelveticaChimicaActa,2016,vol.99,#9,p.665-673

673-32-5    124-38-9    557-20-0    1199-77-5 

[1]HelveticaChimicaActa,2016,vol.99,#9,p.665-673

Downstream Synthesis Route
673-32-5    104830-06-0    139962-70-2 

[1]TetrahedronLetters,1998,vol.39,p.627-630

673-32-5    31930-34-4   
ethyl2-(2',4'-diphenyl-3',5'-dimethyl-1'-cyclopentadienyl)ethanoate 

[1]Tetrahedron,1999,vol.55,p.4969-4978

110-86-1    673-32-5   
ammoniumhydroxide 
 
sulfur 
  102-93-2 

[1]JournaloftheAmericanChemicalSociety,1946,vol.68,p.2029,2032,2755

673-32-5    31930-34-4    266325-19-3 

[1]JournalofOrganicChemistry,2000,vol.65,p.2287-2291

673-32-5    4464-18-0   
1,3,5-Tris-((E)-3-phenyl-allyloxymethyl)-benzene 

[1]TetrahedronLetters,2001,vol.42,p.6207-6210

Literature fold

Title: Phenylpropargyl radicals and their dimerization products: an IR/UV double resonance study.

Journal: The journal of physical chemistry. A20120823

Title: Ab initio/RRKM-ME study on the mechanism and kinetics of the reaction of phenyl radical with 1,2-butadiene.

Journal: The journal of physical chemistry. A20100729

Title: Photoionization of three isomers of the C9H7 radical.

Journal: The journal of physical chemistry. A20100415

Title: Reaction dynamics of phenyl radicals in extreme environments: a crossed molecular beam study.

Journal: Accounts of chemical research20090217

Title: Cross-coupling reaction of alkyl halides with grignard reagents catalyzed by Ni, Pd, or Cu complexes with pi-carbon ligand(s).

Journal: Accounts of chemical research20081118

Title: 1-Phenyl-1-propyne on Cu(111): TOFMS TPD, XPS, UPS, and 2PPE Studies.

Journal: Langmuir : the ACS journal of surfaces and colloids20071120

Title: Copper-catalyzed cross-coupling reaction of grignard reagents with primary-alkyl halides: remarkable effect of 1-phenylpropyne.

Journal: Angewandte Chemie (International ed. in English)20070101

Title: Reactivity of alkynes containing alpha-hydrogen atoms with a triruthenium hydrido carbonyl cluster: alkenyl versus allyl cluster derivatives.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany)20051007

Title: [Ind(2)TiMe(2)]: a general catalyst for the intermolecular hydroamination of alkynes.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany)20040621

Title: Regiochemical variation in the electrophilic addition of HBr to 1-phenylprop-1-yne.

Journal: Organic & biomolecular chemistry20030621

Title: The concerted addition of HBr to aryl alkynes; orthogonal pi bond selectivity.

Journal: Organic & biomolecular chemistry20030621

Title: Cp*(2)TiMe(2): an improved catalyst for the intermolecular addition of n-alkyl- and benzylamines to alkynes.

Journal: The Journal of organic chemistry20020322

Related Products of of 673-32-5
Building Blocks More >
71800-36-7
71800-36-7
LYS-ARG-PRO-PRO-GLY-PHE-SER-PRO-PHE
AA00FAGG | MFCD00079826
669748-48-5
669748-48-5
4-Allyl-5-[4-(diethylamino)phenyl]-4h-1,2,4-triazole-3-thiol
AA00FALB | MFCD03900787
73634-73-8
73634-73-8
GLUFOSINATE-N-ACETYL
AA00FASB | MFCD08273844
730949-79-8
730949-79-8
2-(Difluoromethoxy)-3-methoxybenzaldehyde
AA00FAYV | MFCD04621474
66088-53-7
66088-53-7
1-(2,5-Difluorophenyl)biguanide, HCl
AA00FB7S | MFCD03094448
68506-86-5
68506-86-5
(±)-4-aminohex-5-enoic acid
AA00FBGA | MFCD00274577
66148-17-2
66148-17-2
MYOSMINE-2,4,5,6-D4
AA00FBLR | MFCD02684000
7443-02-9
7443-02-9
(1,3-dioxo-2-phenyl-2,3-dihydro-1H-inden-2-yl)acetic acid
AA00FBRM | MFCD00168641
6877-32-3
6877-32-3
Corynoxine
AA00FBYP | MFCD09953806
65695-05-8
65695-05-8
Methyl 4-(n-hydroxycarbamimidoyl)benzoate
AA00FC3N | MFCD08689689
Historical Records
174219-86-4
174219-86-4
436155-36-1
436155-36-1
1038374-82-1
1038374-82-1
2503-39-1
2503-39-1
341009-06-1
341009-06-1
390-16-9
390-16-9
Submit
© 2017 AA BLOCKS, INC. All rights reserved.