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7517-36-4

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7517-36-4 Usage

Chemical Properties

White Solid

Uses

Dicyclohexyl Phthalate (DCHP) metabolite.

Definition

ChEBI: A phthalic acid monoester resulting from the formal condensation of one of the carboxy groups of phthalic acid with cyclohexanol. It is a metabolite of the commonly used plasticiser dicyclohexyl phthalate.

Check Digit Verification of cas no

The CAS Registry Mumber 7517-36-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,1 and 7 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7517-36:
(6*7)+(5*5)+(4*1)+(3*7)+(2*3)+(1*6)=104
104 % 10 = 4
So 7517-36-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H16O4/c15-13(16)11-8-4-5-9-12(11)14(17)18-10-6-2-1-3-7-10/h4-5,8-10H,1-3,6-7H2,(H,15,16)

7517-36-4 Well-known Company Product Price

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  • Sigma-Aldrich

  • (69262)  mono-Cyclohexyl phthalate  analytical standard

  • 7517-36-4

  • 69262-100MG

  • 1,817.01CNY

  • Detail

7517-36-4SDS

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 2-[(Cyclohexyloxy)carbonyl]benzoic acid

1.2 Other means of identification

Product number -
Other names mono-cyclohexyl phthalate

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:7517-36-4 SDS

7517-36-4Relevant articles and documents

Practical selective monohydrolysis of bulky symmetric diesters: Comparing with sonochemistry

Shi, Jianjun,Zhao, Tian,Niwayama, Satomi

, p. 6815 - 6820 (2018/10/20)

The conditions of the practical selective monohydrolysis of symmetric diesters we previously reported have been modified and applied to selective monohydrolysis of bulky symmetric diesters. While ultrasound is generally considered effective for two-phase reactions, its effect actually turned out to be rather marginal. Instead, use of a larger proportion of a polar aprotic co-solvent, DMSO, and aqueous KOH helped enhance the reaction rates and improve the yields of the half-esters. The reactions are simple, mild and practical without special devices.

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