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3,5-Dimethyl-4-hydroxybenzaldehyde oxime is an organic compound with the chemical formula C9H11NO2. It is derived from 3,5-dimethyl-4-hydroxybenzaldehyde, where an oxime group (-NHOH) replaces one of the hydrogen atoms on the carbonyl group. 3,5-DIMETHYL-4-HYDROXYBENZALDEHYDE OXIME is characterized by its aldehyde and phenolic functional groups, as well as two methyl groups attached to the benzene ring. It is a colorless to pale yellow solid and is soluble in organic solvents. 3,5-Dimethyl-4-hydroxybenzaldehyde oxime is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds due to its versatile chemical structure.

705-49-7

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705-49-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 705-49-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,0 and 5 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 705-49:
(5*7)+(4*0)+(3*5)+(2*4)+(1*9)=67
67 % 10 = 7
So 705-49-7 is a valid CAS Registry Number.

705-49-7SDS

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 3,5-DIMETHYL-4-HYDROXYBENZALDEHYDE OXIME

1.2 Other means of identification

Product number -
Other names 3,5-Dimethyl-4-hydroxy-benzaldoxim

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:705-49-7 SDS

705-49-7Downstream Products

705-49-7Relevant academic research and scientific papers

Hydroxy- or methoxy-substituted benzaldoximes and benzaldehyde-O-alkyloximes as tyrosinase inhibitors

Ley, Jakob P,Bertram, Heinz-Jürgen

, p. 1879 - 1885 (2007/10/03)

Several benzaldoximes, benzaldehyde-O-ethyloximes, and acetophenone-oximes were synthesized and evaluated as tyrosinase inhibitors by an assay based on tyrosinase catalyzed L-DOPA oxidation. Whereas benzaldoxime itself is only a weak inhibitor, its deriva

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