Cas 32999-75-0,3,3-Dimethyl-2-((S)-1-phenyl-ethylamino)-butyric acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester

32999-75-0

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Basic information

Product Name: 3,3-Dimethyl-2-((S)-1-phenyl-ethylamino)-butyric acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester
Synonyms:
CAS NO:32999-75-0
Molecular Formula:
Molecular Weight: 373.579
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: 3,3-Dimethyl-2-((S)-1-phenyl-ethylamino)-butyric acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 3,3-Dimethyl-2-((S)-1-phenyl-ethylamino)-butyric acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester(32999-75-0)
EPA Substance Registry System: 3,3-Dimethyl-2-((S)-1-phenyl-ethylamino)-butyric acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester(32999-75-0)

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: 32999-75-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 32999-75-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,9,9 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 32999-75:
(7*3)+(6*2)+(5*9)+(4*9)+(3*9)+(2*7)+(1*5)=160
160 % 10 = 0
So 32999-75-0 is a valid CAS Registry Number.

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32999-75-0Relevant academic research and scientific papers

Diastereoselective addition of organozinc reagents to chiral α-imino esters

Chiev, Kan Pa,Roland, Sylvain,Mangeney, Pierre

, p. 2205 - 2209 (2002)

The addition of organozinc reagents to chiral α-imino esters pre-complexed with zinc bromide, occurred with complete regioselectivity at the imino carbon. The influence of the solvent, temperature and different chiral auxiliaries was studied. The best diastereoselectivities were obtained in Et2O or CH2Cl2 at 0°C, using phenylglycinol methyl ether as the chiral inductor.

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