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7-[2-[[2-(p-Hydroxyphenyl)-1-methylethyl]amino]ethyl]-1,3-dimethyl-1H-purine-2,6(3H,7H)-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62401-66-5

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62401-66-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62401-66-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,4,0 and 1 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 62401-66:
(7*6)+(6*2)+(5*4)+(4*0)+(3*1)+(2*6)+(1*6)=95
95 % 10 = 5
So 62401-66-5 is a valid CAS Registry Number.
InChI:InChI=1/C18H23N5O3/c1-12(10-13-4-6-14(24)7-5-13)19-8-9-23-11-20-16-15(23)17(25)22(3)18(26)21(16)2/h4-7,11-12,19,24H,8-10H2,1-3H3

62401-66-5SDS

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 7-[2-[1-(4-hydroxyphenyl)propan-2-ylamino]ethyl]-1,3-dimethylpurine-2,6-dione

1.2 Other means of identification

Product number -
Other names p-Hydroxy-fenetyllin

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:62401-66-5 SDS

62401-66-5Downstream Products

62401-66-5Relevant academic research and scientific papers

Investigations on the biotransformation of fenetylline

Rucker,Neugebauer,Heiden

, p. 497 - 501 (2007/10/02)

After oral administration of 3,7-dihydro-1,3-dimethyl-7-2[(1-methyl-2-phenylethyl)-amino-ethyl]-1H -purine-2,6-dione (fenetylline, Captagon), 7 new metabolites could be detected in urine besides 4 known substances. The metabolites were identified by gas chromatography (GC) and by comparison of the mass spectra (MS) of metabolites with those of authentic reference compounds using a combined GC/MS method.

Synthesis of bronchospasmolytically effective β phenylethyl aminoalkyl xanthines

Klingler

, p. 4 - 14 (2007/10/05)

New theophylline and theobromine derivatives are synthesized from the β phenylethylaminoalkyl xanthines, whose phenyl substituent is substituted by one or two hydroxyl groups and partially also by other substituents. Different methods of synthesis are described, among them the production of the bronchospasmolytic 7 (3 [2 (3,5 dihydroxyphenyl) 2 hydroxy ethylamino] propyl) theophylline (reproterol . HCl).

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