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3-bromo-5-tert-butyl-4-hydroxybenzaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65678-06-0

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65678-06-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65678-06-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,6,7 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 65678-06:
(7*6)+(6*5)+(5*6)+(4*7)+(3*8)+(2*0)+(1*6)=160
160 % 10 = 0
So 65678-06-0 is a valid CAS Registry Number.

65678-06-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-bromo-5-tert-butyl-4-hydroxybenzaldehyde

1.2 Other means of identification

Product number -
Other names 3-bromo-5-t-butyl-4- hydroxybenzylaldehyde

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:65678-06-0 SDS

65678-06-0Relevant academic research and scientific papers

Efficient Co(OAc)2-catalyzed aerobic oxidation of EWG-substituted 4-cresols to access 4-hydroxybenzaldehydes

Jiang, Jian-An,Du, Jia-Lei,Liao, Dao-Hua,Wang, Zhan-Guo,Ji, Ya-Fei

supporting information, p. 1406 - 1411 (2014/03/21)

We reported an efficient ligand-free Co(OAc)2·4H 2O/NaOH/O2/ethylene glycol reaction system that enables selective aerobic oxidation of a wide range of substrates covering 2,6-di-EWG-, 2,3,6-tri-EWG-, 2-EWG-, and 2-EWG-6-EDG-substituted 4-cresols into the corresponding 4-hydroxybenzaldehydes. Based on the experimental investigations and well-defined p-benzoquinone methides, a plausible reaction mechanism was proposed. Considering the simplicity of the procedure and importance of the products, the methodology was expected to become a favorable and practical tool in related benzylic C(sp3)-H functionalization chemistry.

Compositions for killing internal parasites containing 3-tert-alkyl-4-hydroxy-5-halo-benzylidene-malonitriles

-

, (2008/06/13)

A compound of the general formula I STR1 wherein R1 is halogen, R4 is a highly branched alkyl group, R2 and R3 which may be the same or different are hydrogen or halogen atoms or lower alkyl groups.

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