Cas 837361-46-3,2H-Isoindole-2-carboxylic acid, 1,3-dihydro-6,7-dimethoxy-1-oxo-, (1S,2R)-2-(1-methyl-1-phenylethyl)cyclohexyl ester

837361-46-3

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Basic information

Product Name: 2H-Isoindole-2-carboxylic acid, 1,3-dihydro-6,7-dimethoxy-1-oxo-, (1S,2R)-2-(1-methyl-1-phenylethyl)cyclohexyl ester
Synonyms:
CAS NO:837361-46-3
Molecular Formula: C26H31NO5
Molecular Weight: 437.536
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: 2H-Isoindole-2-carboxylic acid, 1,3-dihydro-6,7-dimethoxy-1-oxo-, (1S,2R)-2-(1-methyl-1-phenylethyl)cyclohexyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2H-Isoindole-2-carboxylic acid, 1,3-dihydro-6,7-dimethoxy-1-oxo-, (1S,2R)-2-(1-methyl-1-phenylethyl)cyclohexyl ester(837361-46-3)
EPA Substance Registry System: 2H-Isoindole-2-carboxylic acid, 1,3-dihydro-6,7-dimethoxy-1-oxo-, (1S,2R)-2-(1-methyl-1-phenylethyl)cyclohexyl ester(837361-46-3)

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: 837361-46-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 837361-46-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,3,7,3,6 and 1 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 837361-46:
(8*8)+(7*3)+(6*7)+(5*3)+(4*6)+(3*1)+(2*4)+(1*6)=183
183 % 10 = 3
So 837361-46-3 is a valid CAS Registry Number.

837361-46-3Upstream product

837361-46-3Downstream Products

837361-52-1 (3S)-4,5-dimethoxy-1-[6-(2-methoxyethyl)benzo[1,3]dioxol-5-ylmethyl]-3-oxo-1,3-dihydroisoindole-2-carboxylic acid (1S,2R)-2-(1-methyl-1-phenylethyl)cyclohexyl ester

837361-46-3Relevant academic research and scientific papers

Asymmetric synthesis of 3-substituted isoindolinones: Application to the total synthesis of (+)-lennoxamine

Comins, Daniel L.,Schilling, Stefan,Zhang, Yanchen

, p. 95 - 98 (2007/10/03)

(Chemical Equation Presented) An anionic chiral auxiliary mediated asymmetric alkylation of carbamate 2 provides 3-substituted isoindolinones 4 in high ee. This methodology was used in the first asymmetric synthesis of (+)-lennoxamine.

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