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34183-06-7

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34183-06-7 Usage

Preparation

Preparation by Fries rearrangement of 2,6-dichlorophenyl benzoate with aluminium chloride, ? without solvent at 154° for 2.5 h (71%); ? in chlorobenzene at 140–150° for 20 min; ? in nitrobenzene at 75° for 24 h.

Check Digit Verification of cas no

The CAS Registry Mumber 34183-06-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,1,8 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 34183-06:
(7*3)+(6*4)+(5*1)+(4*8)+(3*3)+(2*0)+(1*6)=97
97 % 10 = 7
So 34183-06-7 is a valid CAS Registry Number.
InChI:InChI=1/C13H8Cl2O2/c14-10-6-9(7-11(15)13(10)17)12(16)8-4-2-1-3-5-8/h1-7,17H

34183-06-7SDS

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 (3,5-dichloro-4-hydroxyphenyl)-phenylmethanone

1.2 Other means of identification

Product number -
Other names EINECS 251-866-3

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:34183-06-7 SDS

34183-06-7Relevant articles and documents

An eco-friendly Co(OAc)2-catalyzed aerobic oxidation of 4-benzylphenols into 4-hydroxybenzophenones

Huang, Jian-Gang,Guo, Ying,Jiang, Jian-An,Liu, Hong-Wei,Ji, Ya-Fei

, p. 7115 - 7124 (2015/02/19)

An undecorated Co(OAc)2-catalyzed aerobic oxidation system has been reported that enables direct transformation of 4-benzylphenols into the corresponding 4-hydroxybenzophenones. The procedure is especially suitable for electron-withdrawing group-containing substrates, which are commonly inefficient to conduct this category of oxidation. Based on well-defined p-benzoquinone methides and the confirmed ethereal intermediate, a plausible mechanism was depicted.

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