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62374-32-7

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62374-32-7 Usage

Chemical structure

1,3-Dimethyl-7-(trimethylsilyl)-1H-purine-2,6(3H,7H)-dione

Type of compound

Purine derivative

Functional groups

a. 1,3-Dimethyl groups
b. Trimethylsilyl group
c. 2,6(3H,7H)-dione groups

Role in organic synthesis

Protecting group for hydroxyl functions

Protection mechanism

Trimethylsilyl group shields hydroxyl functionalities

Selectivity

Allows for selective reactions at other sites within the molecule

Applications

a. Pharmaceuticals
b. Agrochemicals
c. Material science

Importance

Intermediate in the production of various chemical compounds

Potential uses

a. Development of new therapeutic agents
b. Study of purine metabolism

Check Digit Verification of cas no

The CAS Registry Mumber 62374-32-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,3,7 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 62374-32:
(7*6)+(6*2)+(5*3)+(4*7)+(3*4)+(2*3)+(1*2)=117
117 % 10 = 7
So 62374-32-7 is a valid CAS Registry Number.

62374-32-7SDS

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 1,3-dimethyl-7-trimethylsilylpurine-2,6-dione

1.2 Other means of identification

Product number -
Other names 7-N-trimethylsilyltheophylline

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:62374-32-7 SDS

62374-32-7Downstream Products

62374-32-7Relevant articles and documents

The synthesis and biological evaluation of nucleobases/tetrazole hybrid compounds: A new class of phosphodiesterase type 3 (PDE3) inhibitors

Shekouhy, Mohsen,Karimian, Somaye,Moaddeli, Ali,Faghih, Zeinab,Delshad, Yousef,Khalafi-Nezhad, Ali

, (2020/05/18)

Spired by the chemical structure of Cilostazol, a selective phosphodiesterase 3A (PDE3A) inhibitor, several novel hybrid compounds of nucleobases (uracil, 6-azauracil, 2-thiuracil, adenine, guanine, theophylline and theobromine) and tetrazole were designe

Silica sulfuric acid (SSA) as a highly efficient heterogeneous catalyst for persilylation of purine and pyrimidine nucleobases and other N-heterocycles using HMDS

Rad, Mohammad Navid Soltani,Khalafi-Nezhad, Ali,Divar, Masoumeh,Behrouz, Somayeh

experimental part, p. 1943 - 1954 (2010/11/16)

Purine and pyrimidine nucleobases and other N-heterocycles have been silylated with HMDS in excellent yields in the presence of a catalytic amount of silica sulfuric acid (SSA) as a heterogeneous catalyst. SSA utilizes a shorter reaction time and higher yields of silylated nucleobases. SSA is reusable for several times without a decrease in reactivity or yield of silylated adducts. Copyright

Synthesis of 8-substituted theophylline β-D-ribofuranosides

Ozola,Ramzaeva,Maurinsh,Lidaks

, p. 827 - 839 (2007/10/02)

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