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80999-72-0

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80999-72-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80999-72-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,9,9 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 80999-72:
(7*8)+(6*0)+(5*9)+(4*9)+(3*9)+(2*7)+(1*2)=180
180 % 10 = 0
So 80999-72-0 is a valid CAS Registry Number.

80999-72-0SDS

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 8-(anilinomethyl)-1,3-dimethyl-7H-purine-2,6-dione

1.2 Other means of identification

Product number -
Other names 1H-Purine-2,6-dione,3,7-dihydro-1,3-dimethyl-8-[(phenylamino)methyl]

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:80999-72-0 SDS

80999-72-0Downstream Products

80999-72-0Relevant articles and documents

A Novel Synthesis of Theophylline Derivatives

Yoneda, Fumio,Koga, Ryosuke

, p. 813 - 816 (2007/10/02)

Treatment of 6-amino-5-arylazo-1,3-dimethyluracils with ethyl propiolate gave the corresponding Michael-type adducts, 5-arylazo-1,3-dimethyl-6-ethoxycarbonylvinylaminouracils, which on treatment with a mixture of hydrochloric acid and acetic acid caused the acid-catalyzed rearrangement accompanied with rearrangement to give rise to the corresponding 8-anilinomethyltheophylline derivatives.In the case that the arylazo group possesses an electron-releasing substituent such as methoxy, the reaction proceeded ina different way to afford 1,2-bis(theophyllin-8-yl)ethane.The presumable reaction mechanisms for the above purine syntheses were proposed.

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