Cas 133390-41-7,6-Methyl-4-phenyl-1,2,3,4-tetrahydro-isoquinoline; hydrochloride

133390-41-7

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Basic information

Product Name: 6-Methyl-4-phenyl-1,2,3,4-tetrahydro-isoquinoline; hydrochloride
Synonyms: 6-Methyl-4-phenyl-1,2,3,4-tetrahydro-isoquinoline; hydrochloride
CAS NO:133390-41-7
Molecular Formula:
Molecular Weight: 259.779
EINECS: N/A
Product Categories: N/A
Mol File: 133390-41-7.mol
Article Data: 1

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: 6-Methyl-4-phenyl-1,2,3,4-tetrahydro-isoquinoline; hydrochloride(CAS DataBase Reference)
NIST Chemistry Reference: 6-Methyl-4-phenyl-1,2,3,4-tetrahydro-isoquinoline; hydrochloride(133390-41-7)
EPA Substance Registry System: 6-Methyl-4-phenyl-1,2,3,4-tetrahydro-isoquinoline; hydrochloride(133390-41-7)

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: 133390-41-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 133390-41-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,3,9 and 0 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 133390-41:
(8*1)+(7*3)+(6*3)+(5*3)+(4*9)+(3*0)+(2*4)+(1*1)=107
107 % 10 = 7
So 133390-41-7 is a valid CAS Registry Number.

133390-41-7Upstream product

133390-40-6 2-(o-aminobenzyl)-4-phenyl-6-methyl-1,2,3,4-tetrahydroisoquinoline dihydrochloride

133390-41-7Downstream Products

133390-41-7Relevant articles and documents

CYCLIZATION OF N-(2-AMINOBENZYL) BENZYLAMINO-1-PHENYL-1-ETHANOLS AND DEBENZYLATION OF THE RESULTING TETRAHYDROISOQUINOLINE DERIVATIVES

Zara-Kaczian, Erzsebet,Deak, Gyula,Szoelloesy, Aron,Brlik, Janos

, p. 743 - 755 (2007/10/02)

Debenzylation reactions of 2-(o-aminobenzyl)-4-phenyl-1,2,3,4-tetrahydroisoquinolines (3a, b) and their N-acetyl derivatives (4a, b), obtained by the cyclization of N-(2-aminobenzyl)benzylamino-1-phenyl-1-ethanols (1), were studied.

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