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Benzenemethanol, 3-amino-2-bromo-4,6-dimethoxy-5-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

873310-48-6

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873310-48-6 Usage

General Description

Benzenemethanol, 3-amino-2-bromo-4,6-dimethoxy-5-methyl- is a complex organic compound with a benzene ring and multiple functional groups. It contains an amino group, a bromine atom, and multiple methoxy groups, as well as a methyl group. Benzenemethanol, 3-amino-2-bromo-4,6-dimethoxy-5-methyl- may be used in organic synthesis or pharmaceutical research due to its unique structure and potential reactivity. Its specific properties and potential applications would need to be further evaluated through detailed chemical analysis and experimentation.

Check Digit Verification of cas no

The CAS Registry Mumber 873310-48-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,3,3,1 and 0 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 873310-48:
(8*8)+(7*7)+(6*3)+(5*3)+(4*1)+(3*0)+(2*4)+(1*8)=166
166 % 10 = 6
So 873310-48-6 is a valid CAS Registry Number.

873310-48-6SDS

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-amino-2-bromo-4,6-dimethoxy-5-methylphenyl)methanol

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:873310-48-6 SDS

873310-48-6Relevant academic research and scientific papers

Efficient construction of novel α-keto spiro ketal and the total synthesis of (±)-terreinol

Wei, Wan-Guo,Zhang, Yong-Xia,Yao, Zhu-Jun

, p. 11882 - 11886 (2007/10/03)

The first total synthesis of (±)-terreinol is described. An intramolecular Pd(II)-catalyzed cycloisomerization of a 2-(1′-alkynyl) benzyl alcohol via an apparent 6-endo diagonal pathway led to the 1H-isochromene ring system, which was further converted to

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