Cas 959975-74-7,(-)-dimethyl (3S,4R)-3-(2-diazo-2-(dimethoxyphosphoryl)ethanoyl)-4-hydroxycyclohexane-1,1-dicarboxylate

959975-74-7

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Basic information

Product Name: (-)-dimethyl (3S,4R)-3-(2-diazo-2-(dimethoxyphosphoryl)ethanoyl)-4-hydroxycyclohexane-1,1-dicarboxylate
Synonyms: (-)-dimethyl (3S,4R)-3-(2-diazo-2-(dimethoxyphosphoryl)ethanoyl)-4-hydroxycyclohexane-1,1-dicarboxylate
CAS NO:959975-74-7
Molecular Formula:
Molecular Weight: 392.303
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: (-)-dimethyl (3S,4R)-3-(2-diazo-2-(dimethoxyphosphoryl)ethanoyl)-4-hydroxycyclohexane-1,1-dicarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (-)-dimethyl (3S,4R)-3-(2-diazo-2-(dimethoxyphosphoryl)ethanoyl)-4-hydroxycyclohexane-1,1-dicarboxylate(959975-74-7)
EPA Substance Registry System: (-)-dimethyl (3S,4R)-3-(2-diazo-2-(dimethoxyphosphoryl)ethanoyl)-4-hydroxycyclohexane-1,1-dicarboxylate(959975-74-7)

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: 959975-74-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 959975-74-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,9,9,7 and 5 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 959975-74:
(8*9)+(7*5)+(6*9)+(5*9)+(4*7)+(3*5)+(2*7)+(1*4)=267
267 % 10 = 7
So 959975-74-7 is a valid CAS Registry Number.

959975-74-7Upstream product

959975-74-7Downstream Products

959975-74-7Relevant academic research and scientific papers

Transformation of fused bicyclic and tricyclic β-lactones to fused γ-lactones and 3(2H)-furanones via ring expansions and O-H insertions

Zhang, Wei,Romo, Daniel

, p. 8939 - 8942 (2007)

(Chemical Equation Presented) A two-step strategy for conversion of β-lactones to γ-lactones and 3(2H)-furanones was developed involving initial acyl C-O cleavage leading to δ-hydroxy-α-diazo-β- ketoesters and β-ketophosphonates. Subsequent tandem Wolff r

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