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3-(5H-purin-6-ylsulfanyl)propane-1,2-diol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91086-60-1

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91086-60-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91086-60-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,0,8 and 6 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 91086-60:
(7*9)+(6*1)+(5*0)+(4*8)+(3*6)+(2*6)+(1*0)=131
131 % 10 = 1
So 91086-60-1 is a valid CAS Registry Number.

91086-60-1SDS

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 3-(7H-purin-6-ylsulfanyl)propane-1,2-diol

1.2 Other means of identification

Product number -
Other names AX 3

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:91086-60-1 SDS

91086-60-1Downstream Products

91086-60-1Relevant academic research and scientific papers

Reactions of SH-substituted purine bases with glycidol

Radchenko,Ratsino

, p. 624 - 626 (2004)

The regioselectivity of S-alkylation of SH-substituted purine bases with glycidol tends to grow with decreasing temperature. A procedure was developed for epoxidation of these compounds in wet liquid ammonia. The products were tested for immunostimulating

SYNTHESIS AND SOME PROPERTIES OF 6-β-OXOALKYL(ARALKYL, HETARALKYL, CYCLOALKYL)THIOPURINES

Kochergin, P. M.,Gromov, M. Yu.,Aleksandrova, E. V.,Skachilova, S. Ya.

, p. 1335 - 1339 (2007/10/02)

The reaction of 6-purinethione with α-haloketones has given a series of new 6-β-oxoalkyl(aralkyl, hetaralkyl, cycloalkyl)thiopurines.Their alkylation in position 9 and acid hydrolysis to hypoxanthine and its 9-alkyl derivatives has been studied.The hydrolysis of the acetals of 6-formylmethylthiopurine and the oxidation of 6-(2,3-dihydroxypropyl)thiopurine leads to 6-formylmethylthiopurine, which shows a ring-chain tautomerism and exists in the form of 7-hydroxy-7,8-dihydrothiazolopurine.

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