Cas 139925-07-8,(4-Chloro-phenyl)-carbamic acid (4S,5S)-2-[(Z)-4-chloro-benzenesulfonylimino]-5-(4-nitro-phenyl)-oxazolidin-4-ylmethyl ester

139925-07-8

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Basic information

Product Name: (4-Chloro-phenyl)-carbamic acid (4S,5S)-2-[(Z)-4-chloro-benzenesulfonylimino]-5-(4-nitro-phenyl)-oxazolidin-4-ylmethyl ester
Synonyms:
CAS NO:139925-07-8
Molecular Formula:
Molecular Weight: 565.391
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: (4-Chloro-phenyl)-carbamic acid (4S,5S)-2-[(Z)-4-chloro-benzenesulfonylimino]-5-(4-nitro-phenyl)-oxazolidin-4-ylmethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (4-Chloro-phenyl)-carbamic acid (4S,5S)-2-[(Z)-4-chloro-benzenesulfonylimino]-5-(4-nitro-phenyl)-oxazolidin-4-ylmethyl ester(139925-07-8)
EPA Substance Registry System: (4-Chloro-phenyl)-carbamic acid (4S,5S)-2-[(Z)-4-chloro-benzenesulfonylimino]-5-(4-nitro-phenyl)-oxazolidin-4-ylmethyl ester(139925-07-8)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 139925-07-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 139925-07-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,9,2 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 139925-07:
(8*1)+(7*3)+(6*9)+(5*9)+(4*2)+(3*5)+(2*0)+(1*7)=158
158 % 10 = 8
So 139925-07-8 is a valid CAS Registry Number.

139925-07-8Upstream product

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139925-07-8Relevant academic research and scientific papers

Synthesis and Spectroscopic Properties of Chiral 1,3-Oxazolidines

Evers, R.,Michalik, M.

, p. 699 - 710 (2007/10/02)

(1S,2S)-2-Amino-1-(p-nitrophenyl)-propane-1,3-diol 2a and the (1R,2R)-configurated isomer 2b react with N-substituted dithiocarbimidic acid diesters and ketenedithioacetals, respectively, to give the 2-substituted chiral 4-hydroxymethyl-5-phenyl-1,3-oxazolidines 4 and 7.N-Carbomethoxy-dithiocarbimidic acid dimethylester yields under the same conditions the isomeric 1,3-oxazolidine 5.On treatment of 4 and 7 with isocyanates crystalline urethanes 9 are formed.

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