Cas 875477-92-2,2,2-Dimethyl-propionic acid (3aS,4R,6S,7R,7aR)-7-hydroxy-2,2-dimethyl-6-p-tolylsulfanyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-4-ylmethyl ester

875477-92-2

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Basic information

Product Name: 2,2-Dimethyl-propionic acid (3aS,4R,6S,7R,7aR)-7-hydroxy-2,2-dimethyl-6-p-tolylsulfanyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-4-ylmethyl ester
Synonyms:
CAS NO:875477-92-2
Molecular Formula:
Molecular Weight: 410.532
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: 2,2-Dimethyl-propionic acid (3aS,4R,6S,7R,7aR)-7-hydroxy-2,2-dimethyl-6-p-tolylsulfanyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-4-ylmethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2,2-Dimethyl-propionic acid (3aS,4R,6S,7R,7aR)-7-hydroxy-2,2-dimethyl-6-p-tolylsulfanyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-4-ylmethyl ester(875477-92-2)
EPA Substance Registry System: 2,2-Dimethyl-propionic acid (3aS,4R,6S,7R,7aR)-7-hydroxy-2,2-dimethyl-6-p-tolylsulfanyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-4-ylmethyl ester(875477-92-2)

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: 875477-92-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 875477-92-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,5,4,7 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 875477-92:
(8*8)+(7*7)+(6*5)+(5*4)+(4*7)+(3*7)+(2*9)+(1*2)=232
232 % 10 = 2
So 875477-92-2 is a valid CAS Registry Number.

875477-92-2Upstream product

875477-92-2Downstream Products

875477-92-2Relevant academic research and scientific papers

Phosphinite thioglycosides derived from natural D-sugars as useful P/S ligands for the synthesis of both enantiomers in palladium-catalyzed asymmetric substitution

Khiar, Noureddine,Suárez, Belén,Valdivia, Victoria,Fernández, Inmaculada

, p. 2963 - 2967 (2005)

Phosphinite thioglycosides I for which a modular synthetic approach is reported, were found highly efficient catalyst precursors for palladium(0)-catalyzed asymmetric substitution. Both enantiomers of the allylated products have been obtained with high ee

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