Cas 1345019-44-4,(-)-3-[(1S)-6,7-dimethoxy-2-[(1S)-1-phenylethyl]-1,2,3,4-tetrahydroisoquinolin-1-yl]propan-1-ol

1345019-44-4

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Basic information

Product Name: (-)-3-[(1S)-6,7-dimethoxy-2-[(1S)-1-phenylethyl]-1,2,3,4-tetrahydroisoquinolin-1-yl]propan-1-ol
Synonyms:
CAS NO:1345019-44-4
Molecular Formula:
Molecular Weight: 355.477
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: (-)-3-[(1S)-6,7-dimethoxy-2-[(1S)-1-phenylethyl]-1,2,3,4-tetrahydroisoquinolin-1-yl]propan-1-ol(CAS DataBase Reference)
NIST Chemistry Reference: (-)-3-[(1S)-6,7-dimethoxy-2-[(1S)-1-phenylethyl]-1,2,3,4-tetrahydroisoquinolin-1-yl]propan-1-ol(1345019-44-4)
EPA Substance Registry System: (-)-3-[(1S)-6,7-dimethoxy-2-[(1S)-1-phenylethyl]-1,2,3,4-tetrahydroisoquinolin-1-yl]propan-1-ol(1345019-44-4)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1345019-44-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1345019-44-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,5,0,1 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1345019-44:
(9*1)+(8*3)+(7*4)+(6*5)+(5*0)+(4*1)+(3*9)+(2*4)+(1*4)=134
134 % 10 = 4
So 1345019-44-4 is a valid CAS Registry Number.

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1345019-44-4Relevant academic research and scientific papers

Electrochemical synthesis and chemistry of chiral 1- cyanotetrahydroisoquinolines. An approach to the asymmetric syntheses of the alkaloid (-)-crispine A and its natural (+)-antipode

Louafi, Fadila,Moreau, Julie,Shahane, Saurabh,Golhen, Stephane,Roisnel, Thierry,Sinbandhit, Sourisak,Hurvois, Jean-Pierre

, p. 9720 - 9732 (2011)

The stereoselective convergent total syntheses of both enantiomers of the tetrahydroisoquinoline (THIQ) alkaloid crispine A are described. The THIQ precursors ( - )-6 (90:10 dr) and ( - )-11 (85:15 dr) were prepared from the alkylation - reduction sequenc

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