Cas 1180844-83-0,(3S,4S)-2-benzyl-4-hydroxymethyl-3-methyl-1,2,3,4-tetrahydroisoquinoline

1180844-83-0

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Basic information

Product Name: (3S,4S)-2-benzyl-4-hydroxymethyl-3-methyl-1,2,3,4-tetrahydroisoquinoline
Synonyms: (3S,4S)-2-benzyl-4-hydroxymethyl-3-methyl-1,2,3,4-tetrahydroisoquinoline
CAS NO:1180844-83-0
Molecular Formula:
Molecular Weight: 267.371
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: (3S,4S)-2-benzyl-4-hydroxymethyl-3-methyl-1,2,3,4-tetrahydroisoquinoline(CAS DataBase Reference)
NIST Chemistry Reference: (3S,4S)-2-benzyl-4-hydroxymethyl-3-methyl-1,2,3,4-tetrahydroisoquinoline(1180844-83-0)
EPA Substance Registry System: (3S,4S)-2-benzyl-4-hydroxymethyl-3-methyl-1,2,3,4-tetrahydroisoquinoline(1180844-83-0)

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: 1180844-83-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1180844-83-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,0,8,4 and 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1180844-83:
(9*1)+(8*1)+(7*8)+(6*0)+(5*8)+(4*4)+(3*4)+(2*8)+(1*3)=160
160 % 10 = 0
So 1180844-83-0 is a valid CAS Registry Number.

1180844-83-0Upstream product

127927-42-8 (2R)-[(1S)-1-(dibenzylamino)ethyl]oxirane

1180844-83-0Downstream Products

1180844-83-0Relevant academic research and scientific papers

Efficient and highly selective synthesis of enantiopure cis-or trans-3,4-disubstituted 1,2,3,4-tetrahydroisoquinolines

Concellon, Jose M.,Tuya, Paula,Del Solar, Virginia,Garcia-Granda, Santiago,Diaz, M. Rosario

, p. 3750 - 3753 (2009)

Image Presented An efficient synthesis of enantiopure 3,4-disubstituted 1,2,3,4-tetrahydroisoquinolines, by treatment of readily available (2R, 1′S)- or (2S, 1′S)-2-(1-aminoalkyl)epoxides with H 3PO4·BF3 complex, under mil

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