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Merck
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주요 문서

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524336

Sigma-Aldrich

4-Bromoindole

96%

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모든 사진(1)

About This Item

실험식(Hill 표기법):
C8H6BrN
CAS Number:
52488-36-5
Molecular Weight:
196.04
MDL number:
MFCD00671502
UNSPSC 코드:
12352100
PubChem Substance ID:
24874403
NACRES:
NA.22

Quality Level

200

분석

96%

refractive index

n20/D 1.655 (lit.)

bp

283-285 °C (lit.)

density

1.563 g/mL at 25 °C (lit.)

작용기

bromo

SMILES string

Brc1cccc2[nH]ccc12

InChI

1S/C8H6BrN/c9-7-2-1-3-8-6(7)4-5-10-8/h1-5,10H

InChI key

GRJZJFUBQYULKL-UHFFFAOYSA-N

애플리케이션

4-Bromoindole may be used to synthesize:
  • clavicipitic acid, an ergot alkaloid
  • 4-bromodehydrotryptophan
  • 3-indolylacetonitrile derivative
  • marine alkaloid dictyodendrin B

픽토그램

Exclamation mark
GHS07

신호어

Warning

유해 및 위험 성명서

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

표적 기관

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

230.0 °F - closed cup

Flash Point (°C)

110 °C - closed cup

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves

가장 최신 버전 중 하나를 선택하세요:

시험 성적서(COA)

Lot/Batch Number
BCBV8218
BCBS3069V
BCBN9165V
BCBH0064V
BCBJ4986V

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문서 라이브러리 방문

이미 열람한 고객

Slide 1 of 3

1 of 3

7-Iodoindole 97%

Sigma-Aldrich

687766

7-Iodoindole

4-Hydroxyindole 99%

Sigma-Aldrich

219878

4-Hydroxyindole

3-(2-Bromoethyl)indole 97%

Sigma-Aldrich

376523

3-(2-Bromoethyl)indole

Optically active total synthesis of clavicipitic acid.
Yokoyama Y, et al.
The Journal of Organic Chemistry, 60(6), 1486-1487 (1995)
Metal-halogen exchange of bromoindoles. A route to substituted indoles.
Moyer MP, et al.
The Journal of Organic Chemistry, 51(26), 5106-5110 (1986)
Andrew K Pitts et al.
Angewandte Chemie (International ed. in English), 54(18), 5451-5455 (2015-02-24)
A sequential CH functionalization strategy for the synthesis of the marine alkaloid dictyodendrin B is reported. Our synthesis begins from commercially available 4-bromoindole and involves six direct functionalizations around the heteroarene core as part of a gram-scale strategy towards the natural
S Liras et al.
Journal of the American Chemical Society, 123(25), 5918-5924 (2001-06-21)
Concise syntheses of the Ergot alkaloids rugulovasine A (3a), rugulovasine B (3b), and setoclavine (2) have been completed by strategies that feature inter- and intramolecular vinylogous Mannich reactions as the key steps. Thus, the first synthesis of 3a,b commenced with
Chaitany Jayprakash Raorane et al.
Biomolecules, 10(8) (2020-08-23)
Multi-drug resistant Acinetobacter baumannii is well-known for its rapid acclimatization in hospital environments. The ability of the bacterium to endure desiccation and starvation on dry surfaces for up to a month results in outbreaks of health care-associated infections. Previously, indole

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