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3-(1-methyl-2-oxocyclohexyl)propanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58625-69-7

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58625-69-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58625-69-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,6,2 and 5 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 58625-69:
(7*5)+(6*8)+(5*6)+(4*2)+(3*5)+(2*6)+(1*9)=157
157 % 10 = 7
So 58625-69-7 is a valid CAS Registry Number.

58625-69-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(1-methyl-2-oxocyclohexyl)propanoic 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:58625-69-7 SDS

58625-69-7Downstream Products

58625-69-7Relevant academic research and scientific papers

Rearrangements of α-Diazo-β-hydroxyketones for the Synthesis of Bicyclo[m.n.1]alkanones

Li, Zhengning,Lam, Shuk Mei,Ip, Ignatius,Wong, Wing-Tak,Chiu, Pauline

, p. 4464 - 4467 (2017/09/11)

Rhodium-catalyzed decomposition of fused bicyclic α-diazo-β-hydroxyketones results in good yields of bridged bicyclo[m.n.1]ketones via a rearrangement pathway.

EFFICIENT SYNTHESIS OF SUBSTITUTED δ-OXO ACIDS

Langlois, Nicole,Dahuron, Nathalie

, p. 7433 - 7436 (2007/10/02)

Activated α,β-unsaturated oxazolines are reactive Michael acceptors in the addition of silyl enol ethers, leading to δ-oxo acids after acidic hydrolysis.

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