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gamma-methyl-1H-indole-3-propanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89229-91-4

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89229-91-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89229-91-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,2,2 and 9 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 89229-91:
(7*8)+(6*9)+(5*2)+(4*2)+(3*9)+(2*9)+(1*1)=174
174 % 10 = 4
So 89229-91-4 is a valid CAS Registry Number.

89229-91-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(1H-indol-3-yl)butan-1-ol

1.2 Other means of identification

Product number -
Other names 1H-Indole-3-propanol,g-methyl

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:89229-91-4 SDS

89229-91-4Downstream Products

89229-91-4Relevant academic research and scientific papers

A Simple and Broadly Applicable C?N Bond Forming Dearomatization Protocol Enabled by Bifunctional Amino Reagents

Ma, Xiaofeng,Farndon, Joshua J.,Young, Tom A.,Fey, Natalie,Bower, John F.

supporting information, p. 14531 - 14535 (2017/10/18)

A C?N bond forming dearomatization protocol with broad scope is outlined. Specifically, bifunctional amino reagents are used for sequential nucleophilic and electrophilic C?N bond formations, with the latter effecting the key dearomatization step. Using t

Highly stereoselective imidazolethiones mediated Friedel-Crafts alkylation of indole derivatives

Liang, Xianrui,Li, Shuangmin,Su, Weike

supporting information; experimental part, p. 289 - 291 (2012/01/31)

The asymmetric Friedel-Crafts alkylation of indoles with α,β-unsaturated aldehydes was promoted by the novel imidazolethiones to afford the corresponding adducts in moderate to excellent yields and high enantioselectivities under mild reaction conditions.

CaSH organocatalysis: Enantioselective Friedel-Crafts alkylation of indoles with α,β-unsaturated aldehydes

Tian, Tian,Pei, Bao-Jian,Li, Qing-Hua,He, Hao,Chen, Ling-Yan,Zhou, Xiang,Chan, Wing-Hong,Lee, Albert W. M.

experimental part, p. 2115 - 2118 (2011/03/22)

Enantioselective Friedel-Crafts alkylation of indole with α,β-unsaturated aldehyde was catalyzed by camphor sulfonyl hydrazine (CaSH) with good enantioselectivity (81-88%). Georg Thieme Verlag Stuttgart.

Enantioselective organocatalytic indole alkylations. Design of a new and highly effective chiral amine for iminium catalysis

Austin, Joel F.,MacMillan, David W. C.

, p. 1172 - 1173 (2007/10/03)

The indole framework has become widely identified as a "privileged" structure with representation in over 3000 natural isolates and 40 medicinal agents of diverse therapeutic action. A new strategy for asymmetric access to this important pharmacaphore has

1-indolyalkyl-4-(substituted-pyridinyl)piperazines

-

, (2008/06/13)

A series of 1,4-disubstituted piperazine derivatives comprised of indol-3-ylalkyl and substituted pyridin-2-yl substituent groups. These compounds are useful as antidepressant agents.

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