Cas 847459-36-3,3-Oxazolidinecarboxylic acid, 2,2,4,4-tetramethyl-, (1S,2R,3E)-2,5-dimethyl-1-[(1S)-1-phenylethyl]-3-hexenyl ester

847459-36-3

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Basic information

Product Name: 3-Oxazolidinecarboxylic acid, 2,2,4,4-tetramethyl-, (1S,2R,3E)-2,5-dimethyl-1-[(1S)-1-phenylethyl]-3-hexenyl ester
Synonyms:
CAS NO:847459-36-3
Molecular Formula: C24H37NO3
Molecular Weight: 387.563
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: 3-Oxazolidinecarboxylic acid, 2,2,4,4-tetramethyl-, (1S,2R,3E)-2,5-dimethyl-1-[(1S)-1-phenylethyl]-3-hexenyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 3-Oxazolidinecarboxylic acid, 2,2,4,4-tetramethyl-, (1S,2R,3E)-2,5-dimethyl-1-[(1S)-1-phenylethyl]-3-hexenyl ester(847459-36-3)
EPA Substance Registry System: 3-Oxazolidinecarboxylic acid, 2,2,4,4-tetramethyl-, (1S,2R,3E)-2,5-dimethyl-1-[(1S)-1-phenylethyl]-3-hexenyl ester(847459-36-3)

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: 847459-36-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 847459-36-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,7,4,5 and 9 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 847459-36:
(8*8)+(7*4)+(6*7)+(5*4)+(4*5)+(3*9)+(2*3)+(1*6)=213
213 % 10 = 3
So 847459-36-3 is a valid CAS Registry Number.

847459-36-3Upstream product

847459-47-6 benzoic acid (2S,3E)-5-methylhex-3-en-2-yl ester

847459-36-3Downstream Products

847459-39-6 (2R,3R,4S)-2-methyl-4-phenylpentane-1,3-diol

847459-36-3Relevant academic research and scientific papers

Nucleophilic addition of α-metallated carbamates to planar chiral cationic η3-allylmolybdenum complexes: A stereochemical study

Kocienski, Philip J.,Christopher, John A.,Bell, Richard,Otto, Bernhard

, p. 75 - 84 (2005)

Chiral α-(O-carbamoyl)alkyl- and α-(N-carbamoyl)alkylcopper(I) reagents derived from (-)-sparteine-mediated asymmetric lithiation of hindered carbamates react with cationic η3-allylmolybdenum complexes with retention of configuration.

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