Cas 1151815-14-3,(4S)-N-[(2R,3R)-2,3-dimethyl-3-methoxy-5-phenylpentanoyl]-4-isopropyl-1,3-thiazolidine-2-thione

1151815-14-3

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Basic information

Product Name: (4S)-N-[(2R,3R)-2,3-dimethyl-3-methoxy-5-phenylpentanoyl]-4-isopropyl-1,3-thiazolidine-2-thione
Synonyms: (4S)-N-[(2R,3R)-2,3-dimethyl-3-methoxy-5-phenylpentanoyl]-4-isopropyl-1,3-thiazolidine-2-thione
CAS NO:1151815-14-3
Molecular Formula:
Molecular Weight: 379.588
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: (4S)-N-[(2R,3R)-2,3-dimethyl-3-methoxy-5-phenylpentanoyl]-4-isopropyl-1,3-thiazolidine-2-thione(CAS DataBase Reference)
NIST Chemistry Reference: (4S)-N-[(2R,3R)-2,3-dimethyl-3-methoxy-5-phenylpentanoyl]-4-isopropyl-1,3-thiazolidine-2-thione(1151815-14-3)
EPA Substance Registry System: (4S)-N-[(2R,3R)-2,3-dimethyl-3-methoxy-5-phenylpentanoyl]-4-isopropyl-1,3-thiazolidine-2-thione(1151815-14-3)

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: 1151815-14-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1151815-14-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,1,8,1 and 5 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1151815-14:
(9*1)+(8*1)+(7*5)+(6*1)+(5*8)+(4*1)+(3*5)+(2*1)+(1*4)=123
123 % 10 = 3
So 1151815-14-3 is a valid CAS Registry Number.

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1151815-14-3Relevant academic research and scientific papers

New approach to the stereoselective synthesis of tertiary methyl ethers

Checa, Begona,Galvez, Erik,Parello, Ricard,Sau, Miriam,Romea, Pedro,Urpi, Felix,Font-Bardia, Merce,Solans, Xavier

supporting information; experimental part, p. 2193 - 2196 (2009/09/28)

The Lewis acid-mediated addition of titanium enolates from 1 to dimethyl ketals of aliphatic methyl ketones followed by removal of the chiral auxiliary furnishes enantiomerically pure derivatives containing a tertiary methyl ether and a contiguous stereoc

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