79944-62-0 Usage
General Description
(3-Chloro-5-nitrophenyl)methanol is a chemical compound which directly belongs to the group of monochlorobenzenes and nitrophenols. It is generally used in the field of synthetic chemistry for various purposes. (3-CHLORO-5-NITROPHENYL)METHANOL, bearing an alcohol functionality on a halogenated nitro aromate, is an essential part in the synthesis of several chemical products. It is generally a light yellow to orange solid with slightly soluble properties in water. Like other chemical compounds, it also needs to be handled with proper safety measures due to its reactive nature in specific conditions.
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
79944-62-0Relevant articles and documents
4-(ORTHO)-FLUOROPHENYL-5-FLUOROPYRIMIDIN-2-YL AMINES CONTAINING A SULFOXIMINE GROUP
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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
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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'.