추천 제품
분석
95%
mp
46-51 °C (lit.)
SMILES string
BrCc1cccc(I)c1
InChI
1S/C7H6BrI/c8-5-6-2-1-3-7(9)4-6/h1-4H,5H2
InChI key
BACZSVQZBSCWIG-UHFFFAOYSA-N
관련 카테고리
일반 설명
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.
애플리케이션
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
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point (°F)
235.4 °F - closed cup
Flash Point (°C)
113 °C - closed cup
개인 보호 장비
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
Phase Transfer Catalyst (PTC) Catalyzed Alkylations of Glycinamides for Asymmetric Syntheses of alpha-Amino Acid Derivatives.
Bull. Korean Chem. Soc., 22(9), 958-962 (2001)
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
Reaction of some sulfonyl halides with trypsin.
Bulletin of the Academy of Sciences of the USSR, Division of chemical science, 22(10), 2251-2254 (1973)
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
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
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