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954-89-2

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954-89-2 Usage

Derivative of indole

Heterocyclic aromatic organic compound

Classification

Substituted indole

Substituents

Methyl group and phenylmethyl group

Appearance

White to light yellow crystalline powder

Primary use

Synthesis of pharmaceuticals and agrochemicals

Versatility

Precursor for the production of various other compounds with potential medicinal and agricultural applications

Check Digit Verification of cas no

The CAS Registry Mumber 954-89-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,5 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 954-89:
(5*9)+(4*5)+(3*4)+(2*8)+(1*9)=102
102 % 10 = 2
So 954-89-2 is a valid CAS Registry Number.

954-89-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-2-methyl-2,3-dihydroindole

1.2 Other means of identification

Product number -
Other names 1H-Indole,2,3-dihydro-2-methyl-1-(phenylmethyl)

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:954-89-2 SDS

954-89-2Relevant articles and documents

One-Pot Transfer Hydrogenation Reductive Amination of Aldehydes and Ketones by Iridium Complexes “on Water”

Ouyang, Lu,Xia, Yanping,Liao, Jianhua,Luo, Renshi

, p. 6387 - 6391 (2020/09/11)

An efficient and practical one-pot transfer hydrogenation reductive amination of aldehydes and ketones with amines has been developed by using iridium complexes as catalysts and formic acid as hydrogen source in aqueous solution, providing an environmentally friendly methodology for the construction of a wide range of functionalized amine compounds in excellent yields (≈ 80 %-95 %). This effective methodology can be scaled up to gram scale with 0.1 mol-% catalyst loading and also be employed in the synthesis of medical substances such as Meclizine.

HMPA-Catalyzed One-Pot Multistep Hydrogenation Method for the Synthesis of 1,2,3-Trisubstituted Indolines

Zhu,Liang,Gong,Pu,Wang,Wang,Zhou,Sun

, p. 452 - 456 (2017/12/27)

A convenient and facile method was developed for the synthesis of 1,2,3-trisubstituted indolines. Starting from indole derivatives and ketones/aldehydes, the corresponding indoline products could be obtained with high yield by the hexamethylphosphoramide (HMPA) catalyzed indole Friedel-Crafts reaction, reduction and direct reductive amination process.

Indolyl derivatives as liver-X-receptor (LXR) modulators

-

Page/Page column 22, (2008/06/13)

The invention relates to compounds of formula (I): and pharmaceutically acceptable salts and pharmaceutically acceptable esters thereof, wherein R1, R2, R3, R4, R5, R6, A, m, n and p are defined as in claim 1. These compounds can be used as pharmaceutical compositions for the treatment of, for example, diabetes.

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