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263164-11-0

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263164-11-0 Usage

General Description

(3S)-3-(1-ethoxyethoxy)-gamma-butyrolactone is a chemical compound with the molecular formula C8H14O4. It is a butyrolactone derivative, which is a type of organic compound. This specific chemical has a stereochemistry of (3S), indicating the configuration of its chiral center. The presence of ethoxyethoxy groups in its structure makes it a potential candidate for use as a solvent, plasticizer, or intermediate in the synthesis of other organic compounds. Its unique structure and properties make it useful in various industrial applications, particularly in the production of polymers and resins. Additionally, it may also have potential uses in pharmaceuticals or other chemical processes. However, like all chemical substances, it should be handled with care and proper safety precautions.

Check Digit Verification of cas no

The CAS Registry Mumber 263164-11-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,3,1,6 and 4 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 263164-11:
(8*2)+(7*6)+(6*3)+(5*1)+(4*6)+(3*4)+(2*1)+(1*1)=120
120 % 10 = 0
So 263164-11-0 is a valid CAS Registry Number.

263164-11-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S)-3-(1-ETHOXYETHOXY)-γ-BUTYROLACTONE

1.2 Other means of identification

Product number -
Other names Fmoc-L-isoasparagine

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:263164-11-0 SDS

263164-11-0Relevant articles and documents

Efficient syntheses of (S)-4-hydroxy-2-pyrrolidinone derivatives

Kanno, Osamu,Miyauchi, Masao,Kawamoto, Isao

, p. 173 - 181 (2007/10/03)

Efficient syntheses of (S)-4-hydroxy-2-pyrrolidinone ((5)-2) and (R)4- acetylthio-2-pyrrolidinone (S), which are key intermediates of oral carbapenem CS-834, were studied. The most efficient route to (S)-2 from (S)- 3-hydroxybutyrolactone (8) was accomplished in high yield via (S)-N-allyl-3- (1-ethoxy)ethoxy-4-hydroxybutyramide (14).

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