Cas 194352-08-4,Carbonic acid (1S,2R)-2-methoxycarbonyloxy-1,2-diphenyl-ethyl ester methyl ester

194352-08-4

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Basic information

Product Name: Carbonic acid (1S,2R)-2-methoxycarbonyloxy-1,2-diphenyl-ethyl ester methyl ester
Synonyms:
CAS NO:194352-08-4
Molecular Formula:
Molecular Weight: 330.337
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: Carbonic acid (1S,2R)-2-methoxycarbonyloxy-1,2-diphenyl-ethyl ester methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Carbonic acid (1S,2R)-2-methoxycarbonyloxy-1,2-diphenyl-ethyl ester methyl ester(194352-08-4)
EPA Substance Registry System: Carbonic acid (1S,2R)-2-methoxycarbonyloxy-1,2-diphenyl-ethyl ester methyl ester(194352-08-4)

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: 194352-08-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 194352-08-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,4,3,5 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 194352-08:
(8*1)+(7*9)+(6*4)+(5*3)+(4*5)+(3*2)+(2*0)+(1*8)=144
144 % 10 = 4
So 194352-08-4 is a valid CAS Registry Number.

194352-08-4Upstream product

194352-08-4Downstream Products

579-43-1 (1S,2R)-1,2-diphenylethane-1,2-diol

194352-08-4Relevant academic research and scientific papers

One-Pot Formation of Carbonates from the Reactions of Carbonyl Compounds with Samarium Diiodide and Methyl Chloroformate

Lu, Ling,Fang, Jim-Min,Lee, Gene-Hsiang,Wang, Yu

, p. 279 - 289 (1997)

Treatment of carbonyl compounds with SmI2 and methyl chloroformate in the presence of molecular sieves provides the cyclic carbonates or biscarbonates of pinacols. This one-pot reaction proceeds rapidly even with aliphatic ketones. The stereoch

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