71636-38-9 Usage
General Description
N-[2-Hydroxy-2-(4-methoxyphenyl)ethyl]-2-(2-chloro-3,4-dimethoxyphenyl)ethylamine is a complex organic compound, which carries certain functional groups like phenyl, chloride, methoxy and amine groups. The compound consists of two aromatic rings, one of which is substituted with a methoxy group and a chloride group, while the other aromatic ring is substituted with a methoxy group. The amine group present gives it basic properties while the methoxy groups may increase its solubility in certain solvents. It is likely synthesized for use in chemical reactions where its structure and properties may be beneficial, such as in the development of pharmaceutical drugs or other specialized chemical products. Without any clear information available, its toxicity and safety data are unknown. Hence, handling and usage should proceed with caution until relevant information becomes available.
Check Digit Verification of cas no
The CAS Registry Mumber 71636-38-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,6,3 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 71636-38:
(7*7)+(6*1)+(5*6)+(4*3)+(3*6)+(2*3)+(1*8)=129
129 % 10 = 9
So 71636-38-9 is a valid CAS Registry Number.
InChI:InChI=1/C19H24ClNO4/c1-23-15-7-4-13(5-8-15)16(22)12-21-11-10-14-6-9-17(24-2)19(25-3)18(14)20/h4-9,16,21-22H,10-12H2,1-3H3
71636-38-9Relevant articles and documents
Process for the preparation of Fenoldopam Mesylate
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Page/Page column 7, (2008/06/13)
Methods and intermediates for the preparation of Fenoldopam mesylate and intermediates thereof are provided.
Chemical processes for 2-(2-halo-3,4-dimethoxybenzyl)-5-(4-methoxyphenyl)oxazolidines
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, (2008/06/13)
New intermediates, namely 2-(2-halo-3,4-dimethoxybenzyl)-5-(4-methoxyphenyl)-oxazolidines, are prepared by a synthetic sequence which uses a Darzen's reaction in a homogeneous solvent system.
Process for preparing secondary amines
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, (2008/06/13)
New intermediates and processes for preparing 6-halo-7,8-dihydroxy-1-(p-hydroxyphenyl)-2,3,4,5-tetrahydro-1H-3-benzazepines involve the reaction of a p-methoxyphenylglyoxal, lower alkyl hemimercaptal with a 2-chloro-3,4-dimethoxyphenethylamine, followed by a borohydride reduction.
