Cas 1407508-23-9,(2R,3S,5R,6R)-5,6-dimethoxy-5,6-dimethyl-1,4-dioxane-2,3-dicarbothioic acid di-S-ethyl ester

1407508-23-9

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Basic information

Product Name: (2R,3S,5R,6R)-5,6-dimethoxy-5,6-dimethyl-1,4-dioxane-2,3-dicarbothioic acid di-S-ethyl ester
Synonyms:
CAS NO:1407508-23-9
Molecular Formula:
Molecular Weight: 352.473
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,3S,5R,6R)-5,6-dimethoxy-5,6-dimethyl-1,4-dioxane-2,3-dicarbothioic acid di-S-ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3S,5R,6R)-5,6-dimethoxy-5,6-dimethyl-1,4-dioxane-2,3-dicarbothioic acid di-S-ethyl ester(1407508-23-9)
EPA Substance Registry System: (2R,3S,5R,6R)-5,6-dimethoxy-5,6-dimethyl-1,4-dioxane-2,3-dicarbothioic acid di-S-ethyl ester(1407508-23-9)

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: 1407508-23-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1407508-23-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,7,5,0 and 8 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1407508-23:
(9*1)+(8*4)+(7*0)+(6*7)+(5*5)+(4*0)+(3*8)+(2*2)+(1*3)=139
139 % 10 = 9
So 1407508-23-9 is a valid CAS Registry Number.

1407508-23-9Upstream product

626201-36-3 (2R,3R,5R,6R)-5,6-dimethoxy-5,6-dimethyl-1,4-dioxane-2,3-dicarbothioic acid di-S-ethyl ester

1407508-23-9Downstream Products

1407508-23-9Relevant academic research and scientific papers

New organocatalysts derived from tartaric and glyceric acids for direct aldol reactions

Maycock, Christopher D.,Rita Ventura

, p. 1262 - 1271 (2012)

The synthesis of several new pyrrolidine based asymmetric organocatalysts derived from tartaric, glyceric acids and a pyrrolidine moiety is described with a study of their application in the development of an enantioselective aldol protocol. The influence

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