Cas 143101-68-2,6H-Purin-6-one, 2-amino-1,9-dihydro-9-[(4-methoxyphenyl)methyl]-8-methyl-, 7-oxide

143101-68-2

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Basic information

Product Name: 6H-Purin-6-one, 2-amino-1,9-dihydro-9-[(4-methoxyphenyl)methyl]-8-methyl-, 7-oxide
Synonyms:
CAS NO:143101-68-2
Molecular Formula: C14H15N5O3
Molecular Weight: 301.305
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 6H-Purin-6-one, 2-amino-1,9-dihydro-9-[(4-methoxyphenyl)methyl]-8-methyl-, 7-oxide(CAS DataBase Reference)
NIST Chemistry Reference: 6H-Purin-6-one, 2-amino-1,9-dihydro-9-[(4-methoxyphenyl)methyl]-8-methyl-, 7-oxide(143101-68-2)
EPA Substance Registry System: 6H-Purin-6-one, 2-amino-1,9-dihydro-9-[(4-methoxyphenyl)methyl]-8-methyl-, 7-oxide(143101-68-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 143101-68-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 143101-68-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,1,0 and 1 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 143101-68:
(8*1)+(7*4)+(6*3)+(5*1)+(4*0)+(3*1)+(2*6)+(1*8)=82
82 % 10 = 2
So 143101-68-2 is a valid CAS Registry Number.

143101-68-2Upstream product

143101-68-2Downstream Products

143101-66-0 8-methylguanine 7-oxide

143101-68-2Relevant academic research and scientific papers

Purines. LII. Synthesis and biological evaluation of 8-methylguanine 7-oxide and its 9-arylmethyl derivatives

Ogawa,Nishii,Inagaki,Nohara,Saito,Itaya,Fujii

, p. 1315 - 1317 (2007/10/02)

The synthesis of 8-methylguanine 7-oxide (3) was accomplished via a 'phenacylamine route', which started from condensation of α-(4-methoxybenzylamino)propiophenone (6), prepared by coupling of α-bromopropiophenone (4) and 4-methoxybenzylamine (5), with 2-

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