Home Halogens t-Butyl bromoacetate

t-Butyl bromoacetate

CAS No.:
5292-43-3
Catalog Number:
AG0035V3
Molecular Formula:
C6H11BrO2
Molecular Weight:
195.0543
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
98%(GC)
In Stock USA
United States
$39
- +
25g
98%(GC)
In Stock USA
United States
$48
- +
100g
98%(GC)
In Stock USA
United States
$85
- +
500g
98%(GC)
In Stock USA
United States
$298
- +
Product Description
Catalog Number:
AG0035V3
Chemical Name:
t-Butyl bromoacetate
CAS Number:
5292-43-3
Molecular Formula:
C6H11BrO2
Molecular Weight:
195.0543
MDL Number:
MFCD00000188
IUPAC Name:
tert-butyl 2-bromoacetate
InChI:
InChI=1S/C6H11BrO2/c1-6(2,3)9-5(8)4-7/h4H2,1-3H3
InChI Key:
BNWCETAHAJSBFG-UHFFFAOYSA-N
SMILES:
BrCC(=O)OC(C)(C)C
EC Number:
226-133-6
NSC Number:
82470
Properties
Complexity:
104  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
193.994g/mol
Formal Charge:
0
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
195.056g/mol
Monoisotopic Mass:
193.994g/mol
Rotatable Bond Count:
3  
Topological Polar Surface Area:
26.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.9  
Literature
Title Journal
tert-Butyl 6-amino-5-cyano-2-(2-meth-oxy-eth-yl)nicotinate. Acta crystallographica. Section E, Structure reports online 20120501
Facile synthesis and evaluation of C-functionalized benzyl-1-oxa-4,7,10-triazacyclododecane-N,N',N″-triacetic acid as chelating agent for ¹¹¹In-labeled polypeptides. Bioorganic & medicinal chemistry 20120115
Amino acid homologation by the Blaise reaction: a new entry into nitrogen heterocycles. The Journal of organic chemistry 20090605
Synthesis of novel 1,4,7,10-tetraazacyclodecane-1,4,7,10-tetraacetic acid (DOTA) derivatives for chemoselective attachment to unprotected polyfunctionalized compounds. Chemistry (Weinheim an der Bergstrasse, Germany) 20070101
Synthesis and application of methyleneoxy pseudodipeptide building blocks in biologically active peptides. Amino acids 20040801
Synthesis and conformational studies of a beta-turn mimetic incorporated in Leu-enkephalin. The Journal of organic chemistry 20040514
Stereoselective synthesis of Psi[CH(2)O] pseudodipeptides and conformational analysis of a PhePsi[CH(2)O]Ala containing analogue of the drug desmopressin. Bioorganic & medicinal chemistry letters 20020325
Asymmetric synthesis of trans-2,3-piperidinedicarboxylic acid and trans-3,4-piperidinedicarboxylic acid derivatives. The Journal of organic chemistry 20020208
Chain extension of sugar delta-lactones with the enolate of tert-butyl bromoacetate and elaboration into functionalized C-ketosides, C-glycosides, and C-glucosyl glycines. Organic letters 20011213
Properties