N-Bromoacetamide
Names
[ CAS No. ]:
79-15-2
[ Name ]:
N-Bromoacetamide
[Synonym ]:
N-BROMOACETAMIDE
N-bromo-acetamide
MFCD00037097
EINECS 201-181-0
sJYHIabIKTp@
Acetamide,N-bromo
Lopac-B-2377
Biological Activity
[Description]:
[Related Catalog]:
[Target]
Sodium channel, Potassium channel[1][2]
[References]
Chemical & Physical Properties
[ Density]:
1.71 g/cm3
[ Melting Point ]:
102-105°C
[ Molecular Formula ]:
C2H4BrNO
[ Molecular Weight ]:
137.96
[ Exact Mass ]:
136.94800
[ PSA ]:
29.10000
[ LogP ]:
0.82330
[ Index of Refraction ]:
1.474
[ Storage condition ]:
−20°C
MSDS
Safety Information
[ Symbol ]:
GHS07
[ Signal Word ]:
Warning
[ Hazard Statements ]:
H315-H319-H335
[ Precautionary Statements ]:
P261-P305 + P351 + P338
[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves
[ Hazard Codes ]:
Xi: Irritant;
[ Risk Phrases ]:
R34
[ Safety Phrases ]:
S26-S36
[ RIDADR ]:
3261
[ WGK Germany ]:
3
[ Packaging Group ]:
III
[ Hazard Class ]:
8
[ HS Code ]:
2924199090
Synthetic Route
Customs
[ HS Code ]: 2924199090
[ Summary ]:
2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%
Articles
Nat. Commun. 6 , 6750, (2015)
During immune reactions, functionally distinct B-cell subsets are generated by stochastic processes, including class-switch recombination (CSR) and plasma cell differentiation (PCD). In this study, we...
Amino Acid-Derived Metabolites from the Ascidian Aplidium sp.Mar. Drugs 13 , 3836-48, (2015)
Four new iodobenzene-containing dipeptides (1-4), a related bromotryptophan-containing dipeptide (5), and an iodophenethylamine (6) were isolated from the ascidian Aplidium sp. collected off the coast...
Aqueous synthesis of N,S-dialkylthiophosphoramidates: design, optimisation and application to library construction and antileishmanial testing.Org. Biomol. Chem. 11(16) , 2660-75, (2013)
We recently reported the use of PSCl3 for the thiophosphorylation of alkylamines where the resulting N-thiophosphoramidate ions could be readily S-alkylated (Chem. Commun., 2011, 47, 6156-6158.). Here...