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Benzenemethanol, 3-nitro-4-(phenylmethoxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

104102-92-3

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104102-92-3 Usage

Chemical properties

nitrophenylmethanol derivative

Uses

precursor in synthesis of pharmaceuticals and commercial products, intermediate in production of organic compounds, potential applications in medicine and biochemistry

Safety precautions

handle with care, follow safety regulations and guidelines to prevent potential hazards

Check Digit Verification of cas no

The CAS Registry Mumber 104102-92-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,1,0 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 104102-92:
(8*1)+(7*0)+(6*4)+(5*1)+(4*0)+(3*2)+(2*9)+(1*2)=63
63 % 10 = 3
So 104102-92-3 is a valid CAS Registry Number.

104102-92-3SDS

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-nitro-4-phenylmethoxyphenyl)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:104102-92-3 SDS

104102-92-3Relevant academic research and scientific papers

Synthesis of Ether Oligomers

Renaudet, Olivier,Reymond, Jean-Louis

, p. 397 - 400 (2007/10/03)

(Equation presented) Hydroxyaromatic aldehydes and ketones were used as building blocks to prepare ether oligomers. An iterative two-step protocol involving Mitsunobu coupling and carbonyl reduction provided a protecting-group-free route with high yields. Activity screening of an 84-member library against proteases led to the discovery of micromolar inhibitors for trypsin, chymotrypsin, and subtilisin.

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