Cas 1139922-15-8,(R)-2-(1,2,3,4-tetrahydroquinolin-2-yl)-1-(3,4-dimethoxyphenyl)ethanone

1139922-15-8

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Basic information

Product Name: (R)-2-(1,2,3,4-tetrahydroquinolin-2-yl)-1-(3,4-dimethoxyphenyl)ethanone
Synonyms: (R)-2-(1,2,3,4-tetrahydroquinolin-2-yl)-1-(3,4-dimethoxyphenyl)ethanone
CAS NO:1139922-15-8
Molecular Formula:
Molecular Weight: 311.381
EINECS: N/A
Product Categories: N/A
Mol File: 1139922-15-8.mol
Article Data: 2

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: (R)-2-(1,2,3,4-tetrahydroquinolin-2-yl)-1-(3,4-dimethoxyphenyl)ethanone(CAS DataBase Reference)
NIST Chemistry Reference: (R)-2-(1,2,3,4-tetrahydroquinolin-2-yl)-1-(3,4-dimethoxyphenyl)ethanone(1139922-15-8)
EPA Substance Registry System: (R)-2-(1,2,3,4-tetrahydroquinolin-2-yl)-1-(3,4-dimethoxyphenyl)ethanone(1139922-15-8)

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: 1139922-15-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1139922-15-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,3,9,9,2 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1139922-15:
(9*1)+(8*1)+(7*3)+(6*9)+(5*9)+(4*2)+(3*2)+(2*1)+(1*5)=158
158 % 10 = 8
So 1139922-15-8 is a valid CAS Registry Number.

1139922-15-8Upstream product

1139922-15-8Downstream Products

608525-32-2 (-)-(2S)-2-[2-(3,4-dimethoxyphenyl)ethyl]-1,2,3,4-tetrahydroquinoline

1139922-15-8Relevant articles and documents

Highly enantioselective Ir-catalyzed hydrogenation of exocyclic enamines

Wang, Xiao-Bing,Wang, Da-Wei,Lu, Sheng-Mei,Yu, Chang-Bin,Zhou, Yong-Gui

experimental part, p. 1040 - 1045 (2009/09/30)

[Ir(COD)Cl]2/MeO-BiPhep/I2 catalyst system is highly effective for the asymmetric hydrogenation of exocyclic enamines with high enantioselectivities (up to 96% ee).

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