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855898-16-7

4,6-diMethyl-heptanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

855898-16-7

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855898-16-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 855898-16-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,5,8,9 and 8 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 855898-16:
(8*8)+(7*5)+(6*5)+(5*8)+(4*9)+(3*8)+(2*1)+(1*6)=237
237 % 10 = 7
So 855898-16-7 is a valid CAS Registry Number.

855898-16-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,6-dimethylheptanoic acid

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:855898-16-7 SDS

855898-16-7Downstream Products

855898-16-7Relevant articles and documents

Directed γ-C(sp3)-H Alkylation of Carboxylic Acid Derivatives through Visible Light Photoredox Catalysis

Chen, Dian-Feng,Chu, John C. K.,Rovis, Tomislav

supporting information, p. 14897 - 14900 (2017/10/31)

Visible light photoredox catalysis enables direct γ- C(sp3)-H alkylation of saturated aliphatic carbonyl compounds. Electron-deficient alkenes are used as the coupling partners in this reaction. Distinguished site selectivity is controlled by the predominant 1,5-hydrogen atom transfer of an amidyl radical generated in situ.

Carboxy-directed asymmetric hydrogenation of 1,1-diarylethenes and 1,1-dialkylethenes

Song, Song,Zhu, Shou-Fei,Yu, Yan-Bo,Zhou, Qi-Lin

, p. 1556 - 1559 (2013/04/24)

Carboxy marks the spot: A carboxy-directed asymmetric hydrogenation of 1,1-diarylethenes and 1,1-dialkylethenes with chiral iridium/spiro phosphine-oxazoline catalysts has been developed. A wide range of chiral diarylethanes and chiral γ-methyl fatty acids were synthesized with excellent enantioselectivity (see scheme). Copyright

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