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106145-23-7

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106145-23-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106145-23-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,1,4 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 106145-23:
(8*1)+(7*0)+(6*6)+(5*1)+(4*4)+(3*5)+(2*2)+(1*3)=87
87 % 10 = 7
So 106145-23-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H11N5O/c1-9-6-5-7(12(2)4-10-6)13(3)8(14)11-5/h4H,1-3H3,(H,11,14)/b9-6-

106145-23-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,9-dimethyl-6-methylimino-7H-purin-8-one

1.2 Other means of identification

Product number -
Other names Caissarone

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:106145-23-7 SDS

106145-23-7Upstream product

106145-23-7Downstream Products

106145-23-7Related news

Increase of mammalian intestinal motility by the iminopurine caissarone (cas 106145-23-7) isolated from the sea anemone Bunodosoma caissarum07/24/2019

The effects of caissarone (C8H11N5O) on guinea-pig ileum and rat duodenum preparations are reported. Caissarone evoked, at first, a small response, as compared with that of applied acetylcholine. This effect was blocked by atropine, hexamethonium and slightly reduced by tetrodotoxin. The main ca...detailed

106145-23-7Relevant academic research and scientific papers

Purines. LVII. Regioselective alkylation of N6,9-disubstituted 8- oxoadenines: Syntheses of the sea anemone purine caissarone and some positional isomers and analogues

Saito,Mori,Chikazawa,Kanai,Fujii

, p. 1746 - 1752 (2007/10/02)

The first total synthesis of caissarone hydrochloride (1), a constituent of the sea anemone Bunodosoma caissarum, has been accomplished via a two- step route starting from N6,9-dimethyl-8-oxoadenine (3), which is obtainable from 9-methyladenine (5) through a four-step route. The key step in the synthesis is the regioselective methylation of 3 at N(3), which has been designed on the basis of a methylation study of N6-benzyl-9-methyl-8- oxoadenine (11). Some positional isomers (19, 24, and 31) and analogues (8, 26, and 32) of 1 have also been synthesized. A 1H-NMR spectroscopic study has suggested that the free base (23) of caissarone is capable of forming a hetero-base pair (such as 41) with 2',3',5'-tri-O-acetylguanosine (40) in Me2SO-d6.

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