Cas 1314102-49-2,(2R,3R,4S,5S,6R)-2-(acetoxymethyl)-6-(3-((1R,2R)-2-(diphenylphosphino)cyclohexyl)thioureido)-tetrahydro-2H-pyran-3,4,5-triyl triacetate

1314102-49-2

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Basic information

Product Name: (2R,3R,4S,5S,6R)-2-(acetoxymethyl)-6-(3-((1R,2R)-2-(diphenylphosphino)cyclohexyl)thioureido)-tetrahydro-2H-pyran-3,4,5-triyl triacetate
Synonyms: (2R,3R,4S,5S,6R)-2-(acetoxymethyl)-6-(3-((1R,2R)-2-(diphenylphosphino)cyclohexyl)thioureido)-tetrahydro-2H-pyran-3,4,5-triyl triacetate
CAS NO:1314102-49-2
Molecular Formula:
Molecular Weight: 672.736
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: (2R,3R,4S,5S,6R)-2-(acetoxymethyl)-6-(3-((1R,2R)-2-(diphenylphosphino)cyclohexyl)thioureido)-tetrahydro-2H-pyran-3,4,5-triyl triacetate(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3R,4S,5S,6R)-2-(acetoxymethyl)-6-(3-((1R,2R)-2-(diphenylphosphino)cyclohexyl)thioureido)-tetrahydro-2H-pyran-3,4,5-triyl triacetate(1314102-49-2)
EPA Substance Registry System: (2R,3R,4S,5S,6R)-2-(acetoxymethyl)-6-(3-((1R,2R)-2-(diphenylphosphino)cyclohexyl)thioureido)-tetrahydro-2H-pyran-3,4,5-triyl triacetate(1314102-49-2)

Safety Data

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Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1314102-49-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1314102-49-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,4,1,0 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1314102-49:
(9*1)+(8*3)+(7*1)+(6*4)+(5*1)+(4*0)+(3*2)+(2*4)+(1*9)=92
92 % 10 = 2
So 1314102-49-2 is a valid CAS Registry Number.

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1314102-49-2Relevant academic research and scientific papers

Enantioselective Morita-Baylis-Hillman reaction organocatalyzed by glucose-based phosphinothiourea

Yang, Weihong,Sha, Feng,Zhang, Xin,Yuan, Kui,Wu, Xinyan

, p. 2652 - 2656 (2013/01/15)

A class of bifunctional phosphinothioureas derived from saccharide was developed as new organocatalysts for the enantioselective Morita-Baylis-Hillman reaction between acrylates and aldehydes. With 10 mol% of glucose-based phosphinothiourea 1d, the allylic alcohols were obtained in up to 96% yield and 83% ee under mild reaction conditions.

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