Cas 1370354-60-1,4-((3-methylthiophen-2-yl)methyl)-2-phenethyl-1,2,3,4-tetrahydroisoquinoline

1370354-60-1

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Basic information

Product Name: 4-((3-methylthiophen-2-yl)methyl)-2-phenethyl-1,2,3,4-tetrahydroisoquinoline
Synonyms: 4-((3-methylthiophen-2-yl)methyl)-2-phenethyl-1,2,3,4-tetrahydroisoquinoline
CAS NO:1370354-60-1
Molecular Formula:
Molecular Weight: 347.524
EINECS: N/A
Product Categories: N/A
Mol File: 1370354-60-1.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: 4-((3-methylthiophen-2-yl)methyl)-2-phenethyl-1,2,3,4-tetrahydroisoquinoline(CAS DataBase Reference)
NIST Chemistry Reference: 4-((3-methylthiophen-2-yl)methyl)-2-phenethyl-1,2,3,4-tetrahydroisoquinoline(1370354-60-1)
EPA Substance Registry System: 4-((3-methylthiophen-2-yl)methyl)-2-phenethyl-1,2,3,4-tetrahydroisoquinoline(1370354-60-1)

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: 1370354-60-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1370354-60-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,0,3,5 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1370354-60:
(9*1)+(8*3)+(7*7)+(6*0)+(5*3)+(4*5)+(3*4)+(2*6)+(1*0)=141
141 % 10 = 1
So 1370354-60-1 is a valid CAS Registry Number.

1370354-60-1Upstream product

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1370354-60-1Relevant articles and documents

Isoquinoline derivatives via stepwise regioselective sp2 and sp3 C-H bond functionalizations

Boudiar, Tarek,Sahli, Zeyneb,Sundararaju, Basker,Achard, Mathieu,Kabouche, Zahia,Doucet, Henri,Bruneau, Christian

experimental part, p. 3674 - 3678 (2012/06/15)

Efficient and practically attractive stepwise ruthenium- and palladium-catalyzed regioselective C-H bond functionalizations were achieved to produce 4-substituted tetrahydroisoquinoline derivatives featuring various heteroaromatic substructures in moderat

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