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13532-34-8

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13532-34-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13532-34-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,5,3 and 2 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 13532-34:
(7*1)+(6*3)+(5*5)+(4*3)+(3*2)+(2*3)+(1*4)=78
78 % 10 = 8
So 13532-34-8 is a valid CAS Registry Number.

13532-34-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-prop-2-enylpurin-6-amine

1.2 Other means of identification

Product number -
Other names 3-allyladenine

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:13532-34-8 SDS

13532-34-8Downstream Products

13532-34-8Relevant articles and documents

-

Tanabe et al.

, p. 259 (1979)

-

Synthesis of N-alkenylpurines by rearrangements of the corresponding N-allyl isomers: Scopes and limitations

Kania, Jindrich,Gundersen, Lise-Lotte

, p. 2008 - 2019 (2013/05/08)

N-9- and N-7-alkenylpurines have been synthesized by rearrangement of the corresponding N-allyl derivatives, often in good yields and with high stereoselectivity. Base promoted and transition metal mediated rearrangements have been studied. Simple allylpurines were easily rearranged with catalytic amounts of RuClH(CO)(PPh3)3. The efficiency of base promoted rearrangement was highly dependent on the detailed structure of the starting material, but this reaction often occurred with surprisingly high Z-selectivity. N-Alkenylpurines have been synthesized, often in good yields, from the corresponding more readily available N-allyl isomers by a double bond migration. The scope and limitation of the rearrangement in the presence of various bases or transition metal complexes have been studied.

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