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931-94-2

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931-94-2 Usage

General Description

1,1-Dimethoxycyclopentane is a chemical compound with the molecular formula C7H14O2. It is a cyclic ether that is commonly used as a solvent in various chemical reactions and processes. This colorless liquid has a boiling point of 126°C and a density of 0.94 g/mL. 1,1-Dimethoxycyclopentane exhibits low reactivity and is considered to be stable under normal conditions. It is also known for its low toxicity and is generally regarded as safe for use in industrial and laboratory settings. Due to its favorable properties, 1,1-Dimethoxycyclopentane is often utilized in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 931-94-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,3 and 1 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 931-94:
(5*9)+(4*3)+(3*1)+(2*9)+(1*4)=82
82 % 10 = 2
So 931-94-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H14O2/c1-8-7(9-2)5-3-4-6-7/h3-6H2,1-2H3

931-94-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1-Dimethoxycyclopentane

1.2 Other means of identification

Product number -
Other names 1,1-DIMETHOXYCYCLOPENTANE

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:931-94-2 SDS

931-94-2Relevant articles and documents

Catalytic asymmetric epoxidation

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Page column 70, (2010/01/30)

A compound and method for producing an enantiomerically enriched epoxide from an olefin using a chiral ketone and an oxidizing agent is disclosed.

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