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166756-77-0

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166756-77-0 Usage

Chemical Properties

white to off-white crystalline powder

Check Digit Verification of cas no

The CAS Registry Mumber 166756-77-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,6,7,5 and 6 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 166756-77:
(8*1)+(7*6)+(6*6)+(5*7)+(4*5)+(3*6)+(2*7)+(1*7)=180
180 % 10 = 0
So 166756-77-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H11NO4/c1-3(5(8)9)2-4(7)6(10)11/h3-4H,2,7H2,1H3,(H,8,9)(H,10,11)/p-1/t3-,4-/m1/s1

166756-77-0SDS

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 (2R,4R)-2-azaniumyl-4-methylpentanedioate

1.2 Other means of identification

Product number -
Other names (2R,4R)-4-Methylglutamic acid hydrochloride

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:166756-77-0 SDS

166756-77-0Downstream Products

166756-77-0Relevant articles and documents

A Highly Diastereoselective Synthesis of 4-Alkyl Threo Glutamic Acids

Gu, Zi-Qiang,Hesson, David P.

, p. 2101 - 2104 (1995)

Treatment of N-p-nitrobenzoyl L- or D-glutamic acid diester with lithium bis(trimethylsilyl)amide generates a chelated γ-enolate which reacts with alkyl halides to give (2S,4S)- or (2R,4R)-4-alkylated glutamic acid derivatives with very high diastereoselectivity.

Stereospecific Synthesis of 4-Alkylglutamates and 4-Alkylprolines

Moody, Claire M.,Young, Douglas W.

, p. 7277 - 7280 (2007/10/02)

Catalytic reduction of the 4-alkylidenepyroglutamate derivatives (3) affords an effective route to (2S,4S)-4-alkylglutamic acids and (2S,4S)-4-alkylprolines.The route has also been used to prepare a 4-alkylpyroglutamic acid derivative which is stereospeci

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