Cas 1198118-25-0,(4R,5R)-methyl 4,5-dimethyl-5-(4-methylphenyl)-2-thioxooxazolidine-4-carboxylate

1198118-25-0

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Basic information

Product Name: (4R,5R)-methyl 4,5-dimethyl-5-(4-methylphenyl)-2-thioxooxazolidine-4-carboxylate
Synonyms: (4R,5R)-methyl 4,5-dimethyl-5-(4-methylphenyl)-2-thioxooxazolidine-4-carboxylate
CAS NO:1198118-25-0
Molecular Formula:
Molecular Weight: 279.36
EINECS: N/A
Product Categories: N/A
Mol File: 1198118-25-0.mol
Article Data: 2

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: (4R,5R)-methyl 4,5-dimethyl-5-(4-methylphenyl)-2-thioxooxazolidine-4-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (4R,5R)-methyl 4,5-dimethyl-5-(4-methylphenyl)-2-thioxooxazolidine-4-carboxylate(1198118-25-0)
EPA Substance Registry System: (4R,5R)-methyl 4,5-dimethyl-5-(4-methylphenyl)-2-thioxooxazolidine-4-carboxylate(1198118-25-0)

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: 1198118-25-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1198118-25-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,8,1,1 and 8 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1198118-25:
(9*1)+(8*1)+(7*9)+(6*8)+(5*1)+(4*1)+(3*8)+(2*2)+(1*5)=170
170 % 10 = 0
So 1198118-25-0 is a valid CAS Registry Number.

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1198118-25-0Relevant articles and documents

Construction of contiguous tetrasubstituted chiral carbon stereocenters via direct catalytic asymmetric aldol reaction of α-isothiocyanato esters with ketones

Yoshino, Tatsuhiko,Morimoto, Hiroyuki,Lu, Gang,Matsunaga, Shigeki,Shibasaki, Masakatsu

, p. 17082 - 17083 (2009)

(Chemical Equation Presented) Construction of contiguous tetrasubstituted chiral carbon stereocenters via direct catalytic asymmetric aldol reaction of α-substituted α-isothiocyanato esters with unactivated simple ketones is described. A Bu2Mg/

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