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125982-19-6

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125982-19-6 Usage

General Description

The chemical compound "(4S)-4-[[(1,1-Dimethylethoxy)carbonyl]amino]-5-hydroxypentanoic acid ethyl ester" is a derivative of 5-hydroxypentanoic acid that is used in the field of organic chemistry and pharmaceutical research. It is an ethyl ester, meaning it contains an ethyl group attached to the carboxylic acid functional group. The compound also contains a carbonyl group and an amino group, which are important for its reactivity and potential biological activity. Overall, this compound is of interest for its potential use as a building block in the synthesis of other organic molecules and for its potential pharmacological properties.

Check Digit Verification of cas no

The CAS Registry Mumber 125982-19-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,9,8 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 125982-19:
(8*1)+(7*2)+(6*5)+(5*9)+(4*8)+(3*2)+(2*1)+(1*9)=146
146 % 10 = 6
So 125982-19-6 is a valid CAS Registry Number.

125982-19-6SDS

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 ethyl (4S)-N-(t-butyloxycarbonyl)amino-5-hydroxypentanoate

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:125982-19-6 SDS

125982-19-6Relevant articles and documents

Enantioselective Synthesis and Absolute Configuration of (-)-α-Kainic Acid

Oppolzer, Wolfgang,Thirring, Klaus

, p. 4978 - 4979 (1982)

-

Conjugate addition to chiral γ-heterosubstituted δ-lactones as pivotal synthons from L-glutamic acid. Synthesis of an optically active lignan lactone; (-)-hinokinin

Yoda,Naito,Takabe,Tanaka,Hosoya

, p. 7623 - 7626 (2007/10/02)

Asymmetric induction in conjugate addition of new chiral γ-heterosubstituted-α, β-unsaturated δ-lactones from L-glutamic acid was accomplished in high diastereoselectivity with the formation of trans-(R,S)-adducts and was disclosed to serve as a versatile procedure for the asymmetric synthesis of antileukemic lignan lactones.

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