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79944-62-0

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79944-62-0 Usage

Description

(3-Chloro-5-nitrophenyl)methanol is a chemical compound that belongs to the group of monochlorobenzenes and nitrophenols. It is characterized by an alcohol functionality on a halogenated nitro aromate, making it an essential component in the synthesis of various chemical products. (3-CHLORO-5-NITROPHENYL)METHANOL is typically a light yellow to orange solid and exhibits slightly soluble properties in water. Due to its reactive nature in specific conditions, it is crucial to handle (3-chloro-5-nitrophenyl)methanol with proper safety measures.

Uses

Used in Synthetic Chemistry:
(3-Chloro-5-nitrophenyl)methanol is used as a key intermediate in the synthesis of several chemical products. Its unique structure allows it to be a valuable building block for creating a wide range of compounds in the field of synthetic chemistry.
Used in Pharmaceutical Industry:
(3-Chloro-5-nitrophenyl)methanol is used as a starting material for the development of new pharmaceutical compounds. Its reactivity and structural features make it a promising candidate for the synthesis of potential drug molecules, contributing to the advancement of medicinal chemistry.
Used in Chemical Research:
(3-Chloro-5-nitrophenyl)methanol is used as a research tool in various chemical studies. Its properties and reactivity are of interest to scientists who aim to understand the behavior of similar compounds and explore their potential applications in different fields.
Used in Material Science:
(3-Chloro-5-nitrophenyl)methanol is used as a component in the development of new materials with specific properties. Its incorporation into the synthesis process can lead to the creation of materials with unique characteristics, such as improved stability or enhanced reactivity, which can be beneficial in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 79944-62-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,9,4 and 4 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 79944-62:
(7*7)+(6*9)+(5*9)+(4*4)+(3*4)+(2*6)+(1*2)=190
190 % 10 = 0
So 79944-62-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H6ClNO3/c8-6-1-5(4-10)2-7(3-6)9(11)12/h1-3,10H,4H2

79944-62-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-CHLORO-5-NITROPHENYL)METHANOL

1.2 Other means of identification

Product number -
Other names 3-CHLORO-5-NITROBENZENEMETHANOL

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:79944-62-0 SDS

79944-62-0Relevant articles and documents

4-(ORTHO)-FLUOROPHENYL-5-FLUOROPYRIMIDIN-2-YL AMINES CONTAINING A SULFOXIMINE GROUP

-

Page/Page column 97, (2014/06/11)

The present invention relates to 4-(ortho)-fluorophenyl-5-fluoropyrimidin-2-yl amine derivatives containing a sulfoximine group of general formula (I) as described and defined herein, and methods for their preparation, their use for the treatment and/or p

PYRROLE DERIVATIVES WITH CRTH2 RECEPTOR MODULATOR ACTIVITY

-

Page/Page column 38, (2008/06/13)

There are provided according to the invention compounds of formula (I) in free or salt form, wherein R3, R 4, R5, R6a, R6b, Q and W are as described in the specification, process for preparing them, a

Enzymatic resolution of substituted mandelic acids

Campbell, Robert F.,Fitzpatrick, Kevin,Inghardt, Tord,Karlsson, Olle,Nilsson, Kristina,Reilly, John E.,Yet, Larry

, p. 5477 - 5481 (2007/10/03)

A series of substituted mandelic acids were prepared and subjected to enzymatic resolution utilizing Lipase PS 'Amano'.

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