427691
3-Iodobenzyl bromide
95%
Sinônimo(s):
α-Bromo-m-iodotoluene, 1-(Bromomethyl)-3-iodobenzene, 3-(Bromomethyl)iodobenzene, m-Iodobenzylbromide
Faça loginpara ver os preços organizacionais e de contrato
About This Item
Fórmula linear:
IC6H4CH2Br
Número CAS:
Peso molecular:
296.93
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22
Ensaio:
95%
Produtos recomendados
Nível de qualidade
Ensaio
95%
pf
46-51 °C (lit.)
grupo funcional
bromo
iodo
cadeia de caracteres SMILES
BrCc1cccc(I)c1
InChI
1S/C7H6BrI/c8-5-6-2-1-3-7(9)4-6/h1-4H,5H2
chave InChI
BACZSVQZBSCWIG-UHFFFAOYSA-N
Categorias relacionadas
Descrição geral
3-Iodobenzyl bromide (3-IBBr, m-iodobenzyl bromide) is a meta-isomer of iodobenzyl bromide. It can be synthesized by the bromination of m-iodotoluene.
Aplicação
3-Iodobenzyl bromide (3-IBBr, m-iodobenzyl bromide) was used as a derivatization reagent for the extraction and purification of thiouracil (TU).
It may be used in the synthesis of the following:
It may be used in the synthesis of the following:
- meta-substituted phenylalanine derivatives
- N6-substituted aristeromycin derivative
- (N)-methanocarba-N6-(3-iodobenzyl)adenosine
Palavra indicadora
Danger
Frases de perigo
Declarações de precaução
Classificações de perigo
Eye Dam. 1 - Skin Corr. 1B
Código de classe de armazenamento
8A - Combustible corrosive hazardous materials
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
235.4 °F - closed cup
Ponto de fulgor (°C)
113 °C - closed cup
Equipamento de proteção individual
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Escolha uma das versões mais recentes:
Já possui este produto?
Encontre a documentação dos produtos que você adquiriu recentemente na biblioteca de documentos.
Julie A L Kiebooms et al.
Applied and environmental microbiology, 80(23), 7433-7442 (2014-09-28)
In recent years, the frequent detection of the banned thyreostat thiouracil (TU) in livestock urine has been related to endogenous TU formation following digestion of glucosinolate-rich Brassicaceae crops. Recently, it was demonstrated that, upon in vitro digestion of Brassicaceae, fecal
Barbara Woźniak et al.
Journal of veterinary research, 62(4), 511-517 (2019-02-08)
In the European Union, the use of thyreostatic drugs for fattening slaughter animals has been banned since 1981 under Council Directive 81/602/EEC. For protection of consumer health against unwanted residues and in compliance with Directive 96/23, each EU country must
Reaction of some sulfonyl halides with trypsin.
Kuranova IP and Konareva NV.
Bulletin of the Academy of Sciences of the USSR, Division of chemical science, 22(10), 2251-2254 (1973)
K A Jacobson et al.
Journal of medicinal chemistry, 43(11), 2196-2203 (2000-06-08)
Adenosine receptor agonists have cardioprotective, cerebroprotective, and antiinflammatory properties. We report that a carbocyclic modification of the ribose moiety incorporating ring constraints is a general approach for the design of A(1) and A(3) receptor agonists having favorable pharmacodynamic properties. While
Phase Transfer Catalyst (PTC) Catalyzed Alkylations of Glycinamides for Asymmetric Syntheses of alpha-Amino Acid Derivatives.
Park YS, et al.
Bull. Korean Chem. Soc., 22(9), 958-962 (2001)
Nossa equipe de cientistas tem experiência em todas as áreas de pesquisa, incluindo Life Sciences, ciência de materiais, síntese química, cromatografia, química analítica e muitas outras.
Entre em contato com a assistência técnica