N-Bromosuccinimide

Suppliers

Names

[ CAS No. ]:
128-08-5

[ Name ]:
N-Bromosuccinimide

[Synonym ]:
2,5-Pyrrolidinedione, bromo-
1-Bromo-2,5-pyrrolidinedione
2,5-Pyrrolidinedione, 1-bromo-
N-bromobutanimide
succinimide, N-bromo-
EINECS 204-877-2
N-Bromosuccinimide
NBS
MFCD00005510
1-Bromopyrrolidine-2,5-dione
Letrozole Impurity 10

Chemical & Physical Properties

[ Density]:
2.0±0.1 g/cm3

[ Boiling Point ]:
221.4±23.0 °C at 760 mmHg

[ Melting Point ]:
175-180 °C (dec.)(lit.)

[ Molecular Formula ]:
C4H4BrNO2

[ Molecular Weight ]:
177.984

[ Flash Point ]:
87.7±22.6 °C

[ Exact Mass ]:
176.942535

[ PSA ]:
37.38000

[ LogP ]:
-0.70

[ Vapour Pressure ]:
0.1±0.4 mmHg at 25°C

[ Index of Refraction ]:
1.606

[ Stability ]:
Stable. Incompatible with strong oxidizing agents, halogenated hydrocarbons.

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS05, GHS07

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H302-H314

[ Precautionary Statements ]:
P280-P305 + P351 + P338-P310

[ Personal Protective Equipment ]:
Eyeshields;Faceshields;full-face particle respirator type N100 (US);Gloves;respirator cartridge type N100 (US);type P1 (EN143) respirator filter;type P3 (EN 143) respirator cartridges

[ Hazard Codes ]:
Xn:Harmful

[ Risk Phrases ]:
R22;R36/37/38

[ Safety Phrases ]:
S26-S36/37/39-S45-S37/39

[ RIDADR ]:
UN 3261 8/PG 2

[ WGK Germany ]:
3

[ Packaging Group ]:
III

[ Hazard Class ]:
8

[ HS Code ]:
2925190090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • Succinimide
  • N-chlorosuccinimide
  • N-Bromoacetamide

DownStream

  • 7-Bromotetraphene
  • 4'-bromo-3'-fluoroacetanilide
  • 3,4-Dihydroisoquinoline
  • ethyl 2-bromo-3-oxo-3-phenylpropanoate
  • 3-thenyl bromide
  • 3H-Pyrazol-3-one,4-bromo-1,2-dihydro-1,5-dimethyl-2-phenyl-
  • 9-Bromophenanthrene
  • 4-BROMO-3-METHYLISOXAZOL-5-AMINE
  • (E)-Ethyl 4-bromobut-2-enoate
  • 9-Bromo-10-(2-naphthyl)anthracene

Customs

[ HS Code ]: 2925190090

[ Summary ]:
2925190090 other imides and their derivatives; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

Articles

Resistance gene analogs involved in tolerant cassava--geminivirus interaction that shows a recovery phenotype.

Virus Genes 51 , 393-407, (2015)

The current literature describes recovery from virus-induced symptoms as a RNA silencing defense, but immunity-related genes, including the structurally specific resistance gene analogs (RGAs) that ma...

Synthesis and Properties of a Novel Pyridineoxazoline Containing Optically Active Helical Polymer as a Catalyst Ligand for Asymmetric Diels-Alder Reaction.

Chirality 27 , 523-31, (2015)

A novel pyridineoxazoline (PyOx) containing helical polymer, poly{(-)-(S)-4-tert-butyl-2-[5-(4-tert-butylphenyl)-3-vinylpyridin-2-yl]-oxazoline} (PA), was designed and synthesized to approach the effe...

Synthesis and In Vitro Evaluation of Thiolated Carrageenan.

J. Pharm. Sci. 104 , 2523-30, (2015)

The aim of this study was to generate and characterize a thiolated carrageenan. Thiolated carrageenan (carrageenan-SH) was synthesized from kappa (κ)- and iota (ι)-carrageenan by bromine replacement o...


More Articles

Related Compounds

  • N-bromosuccinimide
  • N-bromosuccinimide
  • 2,2-dimethyl-N-bromosuccinimide
  • N-hydroxyquinoline-8-sulfonamide
  • N-octanoyl benzotriazole
  • N-[(acetylamino)carbonyl]-2-phenylbutanamide
  • Methyl 2-(4-Methoxyphenyl)thiazole-4-carboxylate
  • 1-(2,6-Difluorobenzoyl)-4-[5-(trifluoromethyl)pyridin-2-yl]piperazine
  • 2-((1-ethyl-5-(p-tolyl)-1H-imidazol-2-yl)thio)-N-(4-methylthiazol-2-yl)acetamide
  • 2-Methyl-4-methylsulfanylpyrazole-3-carboxylic acid
  • 7-Methyl-6-[(2-methylphenyl)methoxy]-1,2-benzisoxazole-3-ethanol
  • N~6~-Ethyl-L-lysine
  • 3,5-Dimethyl-4-((4-((5-methylthiophen-2-yl)sulfonyl)piperazin-1-yl)methyl)isoxazole
  • n-(4-(2-Cyanopropan-2-yl)phenyl)-2-methoxyacetamide
  • 2-[(1R)-1-Methylpropyl]-1H-isoindole-1,3(2H)-dione
  • 3-(2-Chloroethyl)-5,6-diethoxy-1,2-benzisoxazole
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.