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17616-98-7

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17616-98-7 Usage

Chemical Class

Ketones

Contains Methyl and Thienyl Groups

Yes

Usage in Food Industry

Flavoring agent

Usage in Cosmetic Industry

Fragrance ingredient

Other Applications

Solvent in adhesives, paints, and coatings; Organic synthesis and pharmaceutical research

Safety Precautions

Irritating to eyes, skin, and respiratory system; Harmful if ingested or inhaled

Check Digit Verification of cas no

The CAS Registry Mumber 17616-98-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,6,1 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 17616-98:
(7*1)+(6*7)+(5*6)+(4*1)+(3*6)+(2*9)+(1*8)=127
127 % 10 = 7
So 17616-98-7 is a valid CAS Registry Number.

17616-98-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-1-thiophen-2-ylbutan-1-one

1.2 Other means of identification

Product number -
Other names Isovalerothienon

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:17616-98-7 SDS

17616-98-7Downstream Products

17616-98-7Relevant articles and documents

-

Cocker,W. et al.

, p. 1654 - 1659 (1963)

-

Selective, catalytic carbon-carbon bond activation and functionalization promoted by late transition metal catalysts

Bart, Suzanne C.,Chirik, Paul J.

, p. 886 - 887 (2007/10/03)

The selective catalytic activation and functionalization of carbon-carbon bonds in a series of substituted cyclopropane substrates has been developed using commercially available transition metal catalysts. Catalytic hydrogenation and olefination procedures, tolerant of a range of functional groups, have been discovered. Introduction of a chelate-assisting substituent such as [PPh2] is effective in altering the kinetic selectivity and lowering the activation barrier for the catalytic processes. Copyright

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