Cas 79703-32-5,(S)-(-)-2,3,10,11-tetramethoxy-5,6,13,13a-tetrahydroisoquino[3,2-a]isoquinolin-8-one

79703-32-5

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Basic information

Product Name: (S)-(-)-2,3,10,11-tetramethoxy-5,6,13,13a-tetrahydroisoquino[3,2-a]isoquinolin-8-one
Synonyms: (S)-(-)-2,3,10,11-tetramethoxy-5,6,13,13a-tetrahydroisoquino[3,2-a]isoquinolin-8-one
CAS NO:79703-32-5
Molecular Formula:
Molecular Weight: 369.417
EINECS: N/A
Product Categories: N/A
Mol File: 79703-32-5.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: (S)-(-)-2,3,10,11-tetramethoxy-5,6,13,13a-tetrahydroisoquino[3,2-a]isoquinolin-8-one(CAS DataBase Reference)
NIST Chemistry Reference: (S)-(-)-2,3,10,11-tetramethoxy-5,6,13,13a-tetrahydroisoquino[3,2-a]isoquinolin-8-one(79703-32-5)
EPA Substance Registry System: (S)-(-)-2,3,10,11-tetramethoxy-5,6,13,13a-tetrahydroisoquino[3,2-a]isoquinolin-8-one(79703-32-5)

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: 79703-32-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 79703-32-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,7,0 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 79703-32:
(7*7)+(6*9)+(5*7)+(4*0)+(3*3)+(2*3)+(1*2)=155
155 % 10 = 5
So 79703-32-5 is a valid CAS Registry Number.

79703-32-5Upstream product

199742-72-8 1-[2-bromo-4,5-dimethoxybenzyl]-2-[((1S,2R)-(1-methyl-1-phenylethyl)cyclohexyloxy)carbonyl]-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline

79703-32-5Downstream Products

523-02-4 (S)-(-)-norcoralydine

79703-32-5Relevant articles and documents

Chiral auxiliary mediated pictet-spengler reactions: Asymmetric syntheses of (-)-laudanosine, (+)-glaucine and (-)-xylopinine

Comins, Daniel L.,Thakker, Paresh M.,Baevsky, Matthew F.,Badawi, Mohamed M.

, p. 16327 - 16340 (2007/10/03)

Cyclohexyl-based chiral auxiliaries can be used effectively in an asymmetric Pictet-Spengler synthesis of tetrahydroisoquinoline, aporphine and protoberbine alkaloids. Using this strategy, concise asymmetric syntheses of (-)-laudanosine, (+)-glaucine and (+)- xylopinine have been accomplished.

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