Cas 71484-53-2,2-Benzyl-5,7-bis-benzyloxy-1-(3,4,5-trimethoxy-benzyl)-1,2,3,4-tetrahydro-isoquinoline

71484-53-2

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Basic information

Product Name: 2-Benzyl-5,7-bis-benzyloxy-1-(3,4,5-trimethoxy-benzyl)-1,2,3,4-tetrahydro-isoquinoline
Synonyms: 2-Benzyl-5,7-bis-benzyloxy-1-(3,4,5-trimethoxy-benzyl)-1,2,3,4-tetrahydro-isoquinoline
CAS NO:71484-53-2
Molecular Formula:
Molecular Weight: 615.769
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: 2-Benzyl-5,7-bis-benzyloxy-1-(3,4,5-trimethoxy-benzyl)-1,2,3,4-tetrahydro-isoquinoline(CAS DataBase Reference)
NIST Chemistry Reference: 2-Benzyl-5,7-bis-benzyloxy-1-(3,4,5-trimethoxy-benzyl)-1,2,3,4-tetrahydro-isoquinoline(71484-53-2)
EPA Substance Registry System: 2-Benzyl-5,7-bis-benzyloxy-1-(3,4,5-trimethoxy-benzyl)-1,2,3,4-tetrahydro-isoquinoline(71484-53-2)

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: 71484-53-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 71484-53-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,4,8 and 4 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 71484-53:
(7*7)+(6*1)+(5*4)+(4*8)+(3*4)+(2*5)+(1*3)=132
132 % 10 = 2
So 71484-53-2 is a valid CAS Registry Number.

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71484-53-2Relevant academic research and scientific papers

A NEW ONE-POT SYNTHESIS OF 1-ARYLMETHYL-1,2,3,4-TETRAHYDROISOQUINOLINE DERIVATIVES FROM ISOQUINOLINIUM SALTS

Iwakuma, Takeo,Yamada, Koichiro,Itoh, Nobuo,Sugasawa, Shigehiko

, p. 1115 - 1118 (2007/10/02)

There has been described a new one-pot synthesis of 1-arylmethyl-1,2,3,4-tetrahydroisoquinoline derivatives by the Barbier reaction of the quaternary salt (4) with various arylmethyl halides followed by reduction with sodium monoacetoxyborohydride.

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