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1,7-dihydro-1,7-dimethyl-6H-purin-6-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

33155-83-8

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33155-83-8 Usage

Type of Compound

Bitter alkaloid

Natural Sources

Cacao beans, tea leaves

Structural Similarity

Caffeine

Function

Central nervous system stimulant

Additional Effects

Diuretic, cardiovascular, bronchodilator

Medical Applications

Various

Toxicity

Potentially toxic to pets, especially dogs (due to slower metabolism)

Human Consumption

Chocolate and cocoa products

Effects on the Body

Increased heart rate, improved blood flow, relaxation of smooth muscles

Check Digit Verification of cas no

The CAS Registry Mumber 33155-83-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,1,5 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 33155-83:
(7*3)+(6*3)+(5*1)+(4*5)+(3*5)+(2*8)+(1*3)=98
98 % 10 = 8
So 33155-83-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H8N4O/c1-10-3-8-6-5(10)7(12)11(2)4-9-6/h3-4H,1-2H3

33155-83-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,7-dimethylpurin-6-one

1.2 Other means of identification

Product number -
Other names UNII-J9IVN575QZ

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:33155-83-8 SDS

33155-83-8Relevant academic research and scientific papers

Purines. LX. Dimroth rearrangement and concomitant hydrolytic deamination of 7-alkyl-1-methyladenines

Fujii,Saito,Ii,Suzuki

, p. 382 - 384 (2007/10/02)

The Dimroth rearrangement of 7-alkyl-1-methyladenines (8) to produce 7- alkyl-N6-methyladenines (9) (63-72% yield) has been found to be accompanied with unusual hydrolytic deaminations to give 7-alkyl-1-methyl-hypoxanthines (10) (1-3.5%) and/or 7-alkylhypoxanthines (11) (12-22%), when effected in boiling H2O for 4-70 h. Probable pathways leading to these by-products are proposed.

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