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1-Hexanol, 6-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-2-[2-[[(1,1-dimethylethyl)dimethyl silyl]oxy]ethyl]-3-[(4-methoxyphenyl)amino]-, (2S,3R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

837364-65-5

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837364-65-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 837364-65-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,3,7,3,6 and 4 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 837364-65:
(8*8)+(7*3)+(6*7)+(5*3)+(4*6)+(3*4)+(2*6)+(1*5)=195
195 % 10 = 5
So 837364-65-5 is a valid CAS Registry Number.

837364-65-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,3R)-6-(tert-butyldimethylsilyloxy)-2-[(2-tert-butyldimethylsilyloxy)ethyl]-3-(4-methoxyphenylamino)-hexan-1-ol

1.2 Other means of identification

Product number -
Other names -

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:837364-65-5 SDS

837364-65-5Relevant academic research and scientific papers

N,N′-carbonyldiimidazole-mediated cyclization of amino alcohols to substituted azetidines and other N-heterocycles

De Figueiredo, Renata Marcia,Froehlich, Roland,Christmann, Mathias

, p. 4147 - 4154 (2007/10/03)

Amino alcohols are important synthons for N-heterocycles. We have developed an efficient method to activate hydroxyl groups, which avoids the use of toxic reagents and tolerates a wide variety of functional groups. Our strategy has been applied to the syn

A Mannich-cyclization approach for the asymmetric synthesis of saturated N-heterocycles

Münch, Alexander,Wendt, Bianca,Christmann, Mathias

, p. 2751 - 2755 (2007/10/03)

A concise asymmetric synthesis of disubstituted N-heterocycles is reported. Our approach utilizes an optimized Mannich reaction of functionalized aldehydes, followed by a novel dehydrative cyclization mediated by the Staab reagent (1,1′-carbonyldiimidazol

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