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Ethanone, 1-(1,3-oxathiolan-2-yl)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

76887-11-1

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76887-11-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76887-11-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,8,8 and 7 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 76887-11:
(7*7)+(6*6)+(5*8)+(4*8)+(3*7)+(2*1)+(1*1)=181
181 % 10 = 1
So 76887-11-1 is a valid CAS Registry Number.

76887-11-1SDS

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 1-(1,3-oxathiolan-2-yl)ethanone

1.2 Other means of identification

Product number -
Other names 1,3-Oxathiolane,ethanone deriv.

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:76887-11-1 SDS

76887-11-1Downstream Products

76887-11-1Relevant academic research and scientific papers

Reaction of 2-alkoxypropenals with 2-mercaptoethanol

Keiko,Funtikova,Stepanova,Chuvashev,Albanov,Voronkov

, p. 1693 - 1699 (2007/10/03)

The reaction between 2-alkoxypropenals and 2-mercaptoethanol was studied at 20 and 60°C by means of 1HNMR and GC-MS methods. Under kinetically controlled conditions (20°C, 7-30 days) with no catalyst the addition of 2-mercaptoethanol to 2-alkox

Photolysis of 4-Substituted Isoxazolin-5-ones: Sulphur-stabilized Iminocarbenes

Sasaki, Tadashi,Hayakawa, Kenji,Nishida, Sumio

, p. 1054 - 1055 (2007/10/02)

Photolyses of 4-sulphenylated 2,3-dimethylisoxazolin-5-ones proceed via iminocarbene intermediates which are trapped with methanol to give pyruvic aldehyde thioacetals.

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