Cas 133407-70-2,(R)-1-[(4S,5S)-5-(3-Benzyloxy-propyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-2-((R)-toluene-4-sulfinyl)-ethanol

133407-70-2

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Basic information

Product Name: (R)-1-[(4S,5S)-5-(3-Benzyloxy-propyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-2-((R)-toluene-4-sulfinyl)-ethanol
Synonyms: (R)-1-[(4S,5S)-5-(3-Benzyloxy-propyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-2-((R)-toluene-4-sulfinyl)-ethanol
CAS NO:133407-70-2
Molecular Formula:
Molecular Weight: 432.581
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: (R)-1-[(4S,5S)-5-(3-Benzyloxy-propyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-2-((R)-toluene-4-sulfinyl)-ethanol(CAS DataBase Reference)
NIST Chemistry Reference: (R)-1-[(4S,5S)-5-(3-Benzyloxy-propyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-2-((R)-toluene-4-sulfinyl)-ethanol(133407-70-2)
EPA Substance Registry System: (R)-1-[(4S,5S)-5-(3-Benzyloxy-propyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-2-((R)-toluene-4-sulfinyl)-ethanol(133407-70-2)

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: 133407-70-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 133407-70-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,4,0 and 7 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 133407-70:
(8*1)+(7*3)+(6*3)+(5*4)+(4*0)+(3*7)+(2*7)+(1*0)=102
102 % 10 = 2
So 133407-70-2 is a valid CAS Registry Number.

133407-70-2Upstream product

133407-70-2Downstream Products

133407-70-2Relevant academic research and scientific papers

Asymmetric synthesis of the C-3/C-9 fragment of (-) aspicilin

Solladie, Guy,Fernandez, Inmaculada,Maestro, Carmen

, p. 509 - 512 (1991)

The optically active C-3/C-9 fragment of (-) aspicilin is synthesized by reduction of an allylic β-keto sulfoxide followed by hydroxylation of the double bond.

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