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17771-42-5

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17771-42-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17771-42-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,7,7 and 1 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 17771-42:
(7*1)+(6*7)+(5*7)+(4*7)+(3*1)+(2*4)+(1*2)=125
125 % 10 = 5
So 17771-42-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H15N/c1-4-13(2,3)11-9-14-12-8-6-5-7-10(11)12/h4-9,14H,1H2,2-3H3

17771-42-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(3-methylbut-2-enyl)-1H-indole

1.2 Other means of identification

Product number -
Other names 3-Prenylindole

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:17771-42-5 SDS

17771-42-5Relevant articles and documents

Unprecedented total synthesis of bruceolline D, E, and H

Gaikwad, Dnyaneshwar

, p. 3158 - 3164 (2020)

Single pot strategy of wittig olefination-Claisen rearrangement has been employed to obtain 3-prenylated indoles. The resulting indoles on the consecutive sequence of epoxidation, cyclization and further oxidation afforded short, protecting group free tot

Isoprene: A Promising Coupling Partner in C-H Functionalizations

Zhang, Wei-Song,Hu, Yan-Cheng,Chen, Qing-An

, p. 1649 - 1655 (2020/07/24)

Five-carbon dimethylallyl units, such as prenyl and reverse-prenyl, are widely distributed in natural indole alkaloids and terpenoids. In conventional methodologies, these valuable motifs are often derived from substrates bearing leaving groups, but these

An efficient molybdenum(VI)-catalyzed direct substitution of allylic alcohols with nitrogen, oxygen, and carbon nucleophiles

Yang, Hongwei,Fang, Ling,Zhang, Ming,Zhu, Chengjian

experimental part, p. 666 - 672 (2009/07/17)

Direct nucleophilic substitution of allylic alcohols with various nitrogen, oxygen, and carbon nucleophiles catalyzed by MoO2(acac)2 was realized. The corresponding products were obtained in moderate-to-excellent yields. Studies of t

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