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2(3H)-Furanone, 3-butyldihydro-, (S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73746-65-3

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73746-65-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73746-65-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,7,4 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 73746-65:
(7*7)+(6*3)+(5*7)+(4*4)+(3*6)+(2*6)+(1*5)=153
153 % 10 = 3
So 73746-65-3 is a valid CAS Registry Number.

73746-65-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-(+)-2-n-Butyl-γ-butyrolactone

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:73746-65-3 SDS

73746-65-3Downstream Products

73746-65-3Relevant academic research and scientific papers

Asymmetric Synthesis of 2-Substituted Butyrolactones and Valerolactones

Meyers, A. I.,Yamamoto, Yukio,Mihelich, Edward D.,Bell, Richard A.

, p. 2792 - 2796 (2007/10/02)

The use of chiral oxazolines 1, 2, 5, and 8 under asymmetrically induced alkylation conditions gave α-substituted oxazolines 3, 6, 9, and 13 which were hydrolyzed to α-substituted butyro- and valerolactones 4 and 11.Either enantiomer of the lactones could be prepared in predictable absolute configuration by reversing the order of alkyl group introduction.The lactones were prepared in 60-86 percent enantiomeric excess which was determined by either chemical correlation or high-pressure liquid chromatography of the diastereomers 10.

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