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99237-42-0

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99237-42-0 Usage

Uses

Production of dyes
Pharmaceuticals
Photographic developers
Reducing agent in organic compound synthesis

Health Hazards

Skin and eye irritation
Harmful if ingested, inhaled, or absorbed through the skin

Importance

Despite hazards, remains crucial in various industrial applications

Check Digit Verification of cas no

The CAS Registry Mumber 99237-42-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,2,3 and 7 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 99237-42:
(7*9)+(6*9)+(5*2)+(4*3)+(3*7)+(2*4)+(1*2)=170
170 % 10 = 0
So 99237-42-0 is a valid CAS Registry Number.

99237-42-0SDS

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 [4-(hydroxyamino)phenyl]methanol

1.2 Other means of identification

Product number -
Other names Benzenemethanol,4-(hydroxyamino)

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:99237-42-0 SDS

99237-42-0Relevant articles and documents

Self-immolative prodrugs: Candidates for antibody-directed enzyme prodrug therapy in conjunction with a nitroreductase enzyme

Mauger,Burke,Somani,Friedlos,Knox

, p. 3452 - 3458 (1994)

The synthesis and properties of some prodrug candidates for antibody- directed enzyme prodrug therapy (ADEPT) are described. These compounds have been designed to generate the corresponding active drug upon interaction with a bacterial nitroreductase that

Leaving group effects in reductively triggered fragmentation of 4-nitrobenzyl carbamatesf

Sykes, Bridget M.,Hay, Michael P.,Bohinc-Herceg, Dubravka,Helsby, Nuala A.,O'Connor, Charmian J.,Denny, William A.

, p. 1601 - 1608 (2007/10/03)

The rates and extent of release of a series of substituted anilines from 4-nitrobenzyl carbamates, following nitro group reduction by radiolytic, enzymic and chemical methods, are reported. The yield of released anilines decreased over the pH range 4-7, b

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