Cas 756524-32-0,Acetic acid (S)-1-((2R,3S)-3-hydroxymethyl-oxiranylmethyl)-3-(4-methoxy-benzyloxy)-propyl ester

756524-32-0

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Basic information

Product Name: Acetic acid (S)-1-((2R,3S)-3-hydroxymethyl-oxiranylmethyl)-3-(4-methoxy-benzyloxy)-propyl ester
Synonyms: Acetic acid (S)-1-((2R,3S)-3-hydroxymethyl-oxiranylmethyl)-3-(4-methoxy-benzyloxy)-propyl ester
CAS NO:756524-32-0
Molecular Formula:
Molecular Weight: 324.374
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: Acetic acid (S)-1-((2R,3S)-3-hydroxymethyl-oxiranylmethyl)-3-(4-methoxy-benzyloxy)-propyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid (S)-1-((2R,3S)-3-hydroxymethyl-oxiranylmethyl)-3-(4-methoxy-benzyloxy)-propyl ester(756524-32-0)
EPA Substance Registry System: Acetic acid (S)-1-((2R,3S)-3-hydroxymethyl-oxiranylmethyl)-3-(4-methoxy-benzyloxy)-propyl ester(756524-32-0)

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: 756524-32-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 756524-32-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,5,6,5,2 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 756524-32:
(8*7)+(7*5)+(6*6)+(5*5)+(4*2)+(3*4)+(2*3)+(1*2)=180
180 % 10 = 0
So 756524-32-0 is a valid CAS Registry Number.

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756524-32-0Relevant academic research and scientific papers

Total synthesis of the salicylate enamide macrolide oximidine III: Application of relay ring-closing metathesis

Wang, Xiang,Bowman, Emma Jean,Bowman, Barry J.,Porco Jr., John A.

, p. 3601 - 3605 (2007/10/03)

The vacuolar-type (H+)-adenosine triphosphatase inhibitor oximidine III and its enamide and epoxide stereoisomers have been synthesized enantioselectively. A relay ring-closing metathesis (RCM) strategy was employed to facilitate the macrocycli

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