Home Other Building Blocks 21075-83-2
21075-83-2,MFCD05669700
Catalog No.:AA002KV7

21075-83-2 | 1-Boc-1-methylhydrazine

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
97%
in stock  
$6.00   $4.00
- +
5g
97%
in stock  
$7.00   $5.00
- +
10g
97%
in stock  
$12.00   $8.00
- +
25g
95%
in stock  
$17.00   $12.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA002KV7
Chemical Name:
1-Boc-1-methylhydrazine
CAS Number:
21075-83-2
Molecular Formula:
C6H14N2O2
Molecular Weight:
146.1876
MDL Number:
MFCD05669700
SMILES:
O=C(N(N)C)OC(C)(C)C
Properties
Properties
 
BP:
186℃  
Form:
Liquid  
Refractive Index:
n20/D 1.436  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
128  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
2  
XLogP3:
0.4  

Upstream Synthesis Route

[1]BioorganicandMedicinalChemistryLetters,2003,vol.13,#14,p.2413-2418

[2]Chirality,2013,vol.25,#6,p.341-349

[3]JournalofAntibiotics,1993,vol.46,#8,p.1279-1288

[4]Patent:US5275816,1994,A,

[5]BioorganicChemistry,2010,vol.38,#5,p.229-233

[6]BioorganicandMedicinalChemistry,2014,vol.22,#15,p.4162-4176

[7]Patent:US2007/49632,2007,A1,.Locationinpatent:Page/Pagecolumn11

[8]Patent:US2005/256107,2005,A1,.Locationinpatent:Page/Pagecolumn53

[9]ChemischeBerichte,1982,vol.115,#8,p.2807-2818

[10]JournalofHeterocyclicChemistry,2000,vol.37,#1,p.47-55

[11]Patent:CN108178740,2018,A,.Locationinpatent:Paragraph0033;0034

[12]ChemMedChem,2013,vol.8,#8,p.1314-1321

[13]TheJournaloforganicchemistry,2002,vol.67,#25,p.8962-8969

[14]OrganicLetters,2015,vol.17,#2,p.254-257

[15]ACSMedicinalChemistryLetters,2014,vol.5,#10,p.1076-1081

[16]Patent:US6413997,2002,B1,

[17]Patent:US6015826,2000,A,

[18]ChemicalCommunications,2012,vol.48,#46,p.5772-5774

[19]JournalofOrganicChemistry,1999,vol.64,#1,p.276-281

[20]JournalofOrganicChemistry,2005,vol.70,#26,p.10701-10708

[21]Patent:US4904775,1990,A,

[22]Patent:US5030724,1991,A,

[23]Patent:US5112968,1992,A,

[24]JournalofMedicinalChemistry,2008,vol.51,#4,p.924-931

[25]Patent:WO2005/87764,2005,A1,.Locationinpatent:Page/Pagecolumn26

[26]BioorganicandMedicinalChemistry,2015,vol.23,#15,p.4952-4969

[27]JournalofMedicinalChemistry,2016,vol.59,#12,p.5799-5809

[28]Patent:WO2005/123717,2005,A1,.Locationinpatent:Page/Pagecolumn16;18

[1]Patent:CN108129357,2018,A,.Locationinpatent:Paragraph0102;0104

[2]EuropeanJournalofOrganicChemistry,2010,#20,p.3815-3822

[1]Patent:WO2007/139346,2007,A1,.Locationinpatent:Page/Pagecolumn49

[1]ChemMedChem,2018,vol.13,#16,p.1681-1694

[2]TetrahedronLetters,2000,vol.41,#2,p.205-207

[3]JournalofOrganicChemistry,2000,vol.65,#14,p.4370-4374

[1]JournaloftheAmericanChemicalSociety,2006,vol.128,#17,p.5646-5647

Downstream Synthesis Route
59483-84-0    127799-54-6    21075-83-2   
Boc-Alaa-Alaa-Boc 

[1]JournaloftheAmericanChemicalSociety,1996,vol.118,p.2539-2544

59483-84-0    21075-83-2   
Boc-Alaa-Alaa-Boc 

[1]JournaloftheAmericanChemicalSociety,1996,vol.118,p.2539-2544

[1]Kelly,T.Ross;Elliott,EricL.;Lebedev,Rimma;Pagalday,Jaione[JournaloftheAmericanChemicalSociety,2006,vol.128,#17,p.5646-5647]

[1]Brosse,Nicolas;Pinto,Maria-Fatima;Jamart-Gregoire,Brigitte[JournalofOrganicChemistry,2000,vol.65,#14,p.4370-4374]

[2]Brosse,Nicolas;Pinto,Maria-Fatima;Jamart-Grégoire,Brigitte[TetrahedronLetters,2000,vol.41,#2,p.205-207]

[3]Matheson,ChristopherJ.;Casalvieri,KimberlyA.;Backos,DonaldS.;Reigan,Philip[ChemMedChem,2018,vol.13,#16,p.1681-1694]

[4]CurrentPatentAssignee:UNIVERSITYOFCOLORADO(SYSTEM)-WO2019/169065,2019,A2

21075-83-2    213211-69-9   
N'-(2-ethoxy-phenyl)-N-methyl-hydrazinecarboxylicacidtert-butylester 

[1]Patent:US2007/49632,2007,A1.Locationinpatent:Page/Pagecolumn73

Literature
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SDS
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