Cas 392662-76-9,Isoquinoline, 1,2,3,4-tetrahydro-6,7-dimethoxy-1-(1-methylethyl)-2-[(R)-(4-methylphen yl)sulfinyl]-, (1R)-

392662-76-9

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Basic information

Product Name: Isoquinoline, 1,2,3,4-tetrahydro-6,7-dimethoxy-1-(1-methylethyl)-2-[(R)-(4-methylphen yl)sulfinyl]-, (1R)-
Synonyms:
CAS NO:392662-76-9
Molecular Formula: C21H27NO3S
Molecular Weight: 373.516
EINECS: N/A
Product Categories: N/A
Mol File: 392662-76-9.mol

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: Isoquinoline, 1,2,3,4-tetrahydro-6,7-dimethoxy-1-(1-methylethyl)-2-[(R)-(4-methylphen yl)sulfinyl]-, (1R)-(CAS DataBase Reference)
NIST Chemistry Reference: Isoquinoline, 1,2,3,4-tetrahydro-6,7-dimethoxy-1-(1-methylethyl)-2-[(R)-(4-methylphen yl)sulfinyl]-, (1R)-(392662-76-9)
EPA Substance Registry System: Isoquinoline, 1,2,3,4-tetrahydro-6,7-dimethoxy-1-(1-methylethyl)-2-[(R)-(4-methylphen yl)sulfinyl]-, (1R)-(392662-76-9)

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: 392662-76-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 392662-76-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,2,6,6 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 392662-76:
(8*3)+(7*9)+(6*2)+(5*6)+(4*6)+(3*2)+(2*7)+(1*6)=179
179 % 10 = 9
So 392662-76-9 is a valid CAS Registry Number.

392662-76-9Upstream product

392662-76-9Downstream Products

392662-76-9Relevant academic research and scientific papers

Enantiopure tetrahydroisoquinolines via N-sulfinyl Pictet-Spengler reactions

Gremmen, Christiaan,Wanner, Martin J,Koomen, Gerrit-Jan

, p. 8885 - 8888 (2007/10/03)

Asymmetric Pictet-Spengler reactions with (R)-N-p-tolylsulfinyl-3,4-dimethoxyphenylethyl amine proceeded with high diastereoselectivity. Starting from the commercially available (R)- and (S)-Andersen reagents a highly efficient route to (+)- and (-)-salsolidine and related tetrahydroisoquinolines was developed.

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