추천 제품
vapor pressure
40 mmHg ( 96 °C)
Quality Level
제품 라인
ReagentPlus®
분석
99%
형태
crystals
bp
190 °C (lit.)
mp
88-90 °C (lit.)
SMILES string
BrC(Br)(Br)Br
InChI
1S/CBr4/c2-1(3,4)5
InChI key
HJUGFYREWKUQJT-UHFFFAOYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
관련 카테고리
일반 설명
Tetrabromomethane can serve as a mediator, catalyst, and reagent in the synthesis of valuable chemicals.
애플리케이션
Tetrabromomethane may be used in the following applications:
- As a transfer agent for the copolymerization of methylmethacrylate and p-divinylbenzene to form soluble crosslinked polymers.
- As a catalyst for the aerobic photooxidative synthesis of aromatic esters from benzyl alcohols under metal-free conditions.
- Bromination of adamantane and its derivatives in the presence of iron compounds as catalyst.
법적 정보
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
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.
이미 열람한 고객
Preparation of soluble microgel by the copolymerization of methylmethacrylate with p?divinylbenzene in the presence of tetrabromomethane.
Journal of Polymer Science Part A: Polymer Chemistry, 22(9), 2123-2130 (1984)
Recent advances in the application of tetrabromomethane in organic synthesis
Inorganic chemistry frontiers, 8(15), 4288-4314 (2021)
Bromination of adamantane and its derivatives with tetrabromomethane catalyzed by iron compounds.
Russ. J. Org. Chem., 51(2), 184-187 (2015)
Aerobic oxidative esterification of benzyl alcohols with catalytic tetrabromomethane under visible light irradiation.
Tetrahedron Letters, 53(39), 5306-5308 (2012)
Organic & biomolecular chemistry, 1(14), 2518-2521 (2003-09-06)
The reaction of a 2-O-benzyl-1-hydroxy sugar with CBr4 and Ph3P generates a glycosyl bromide in situ, which is coupled with an acceptor alcohol in the presence of N,N-tetramethylurea to afford an alpha-glycosyl product virtually quantitatively. In a proposed pathway, the
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