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28353-00-6

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28353-00-6 Usage

General Description

Cyclobutaneacetonitrile, 3-acetyl-2,2-dimethyl-, (1R,3R)-rel- is a chemical compound with the molecular formula C9H15NO. It is a chiral compound, meaning it has a non-superimposable mirror image, and is used in the production of pharmaceuticals and agrochemicals. The compound is a cyclobutanone derivative and is commonly used as an intermediate in organic synthesis. It is also known for its potential use in the development of new drugs and therapeutic agents due to its unique structural properties. The stereoisomeric nature of the compound and its potential applications make it an important chemical in the field of organic chemistry and drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 28353-00-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,3,5 and 3 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 28353-00:
(7*2)+(6*8)+(5*3)+(4*5)+(3*3)+(2*0)+(1*0)=106
106 % 10 = 6
So 28353-00-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H14O.C2H3N/c1-6(9)7-4-5-8(7,2)3;1-2-3/h7H,4-5H2,1-3H3;1H3/t7-;/m1./s1

28353-00-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name acetonitrile,1-(2,2-dimethylcyclobutyl)ethanone

1.2 Other means of identification

Product number -
Other names ethanenitrile

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:28353-00-6 SDS

28353-00-6Downstream Products

28353-00-6Relevant articles and documents

Conversion of Terpenic Compounds to ω-Ketonitriles

Tkachev, A.V.,Rukavishnikov, A.V.,Chibirjaev, A.M.,Volodarsky, L.B.

, p. 2123 - 2132 (2007/10/02)

Conversion of unsaturated terpenoids with trisubstituted carbon-carbon double bond into α-aminooximes followed by treatment with phosphorus pentachloride results in the formation of seco-terpenic ω-ketonitriles.

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