Cas 1088481-64-4,(2R)-2-(5'-tert-butoxycarbonyl-2'-methylphenyl)-2-dimethylamino-4-methylpent-4-enoic acid (-)-8-phenylmenthol ester

1088481-64-4

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Basic information

Product Name: (2R)-2-(5'-tert-butoxycarbonyl-2'-methylphenyl)-2-dimethylamino-4-methylpent-4-enoic acid (-)-8-phenylmenthol ester
Synonyms: (2R)-2-(5'-tert-butoxycarbonyl-2'-methylphenyl)-2-dimethylamino-4-methylpent-4-enoic acid (-)-8-phenylmenthol ester
CAS NO:1088481-64-4
Molecular Formula:
Molecular Weight: 561.805
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: (2R)-2-(5'-tert-butoxycarbonyl-2'-methylphenyl)-2-dimethylamino-4-methylpent-4-enoic acid (-)-8-phenylmenthol ester(CAS DataBase Reference)
NIST Chemistry Reference: (2R)-2-(5'-tert-butoxycarbonyl-2'-methylphenyl)-2-dimethylamino-4-methylpent-4-enoic acid (-)-8-phenylmenthol ester(1088481-64-4)
EPA Substance Registry System: (2R)-2-(5'-tert-butoxycarbonyl-2'-methylphenyl)-2-dimethylamino-4-methylpent-4-enoic acid (-)-8-phenylmenthol ester(1088481-64-4)

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: 1088481-64-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1088481-64-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,8,8,4,8 and 1 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1088481-64:
(9*1)+(8*0)+(7*8)+(6*8)+(5*4)+(4*8)+(3*1)+(2*6)+(1*4)=184
184 % 10 = 4
So 1088481-64-4 is a valid CAS Registry Number.

1088481-64-4Upstream product

1088481-58-6 N-{(S)-(5'-tert-butoxycarbonyl-2'-methylphenyl)[(-)-8-phenylmenthyloxycarbonyl]methyl}-N,N-dimethyl-N-(2-methylprop-2-en-1-yl)ammonium bromide

1088481-64-4Downstream Products

1088481-64-4Relevant academic research and scientific papers

New synthetic routes to optically active α-quaternary α-aryl amino acid derivatives via the diastereoselective Stevens and Sommelet-Hauser rearrangements

Tayama, Eiji,Orihara, Kiwako,Kimura, Hiroshi

experimental part, p. 3673 - 3680 (2009/02/05)

The Stevens rearrangement of N-allylic α-aryl amino acid-derived ammonium salts and the Sommelet-Hauser rearrangement of N-benzylic α-alkyl amino acid-derived ammonium salts are shown to proceed with remarkably high levels of diastereoselectivity. The met

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