Cas 1319741-06-4,(R)-1-methoxy-1-oxo-3-(trityloxy)propan-2-yl 3-oxo-3-(phenylthio)propanoate

1319741-06-4

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Basic information

Product Name: (R)-1-methoxy-1-oxo-3-(trityloxy)propan-2-yl 3-oxo-3-(phenylthio)propanoate
Synonyms: (R)-1-methoxy-1-oxo-3-(trityloxy)propan-2-yl 3-oxo-3-(phenylthio)propanoate
CAS NO:1319741-06-4
Molecular Formula:
Molecular Weight: 540.637
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-methoxy-1-oxo-3-(trityloxy)propan-2-yl 3-oxo-3-(phenylthio)propanoate(CAS DataBase Reference)
NIST Chemistry Reference: (R)-1-methoxy-1-oxo-3-(trityloxy)propan-2-yl 3-oxo-3-(phenylthio)propanoate(1319741-06-4)
EPA Substance Registry System: (R)-1-methoxy-1-oxo-3-(trityloxy)propan-2-yl 3-oxo-3-(phenylthio)propanoate(1319741-06-4)

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: 1319741-06-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1319741-06-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,9,7,4 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1319741-06:
(9*1)+(8*3)+(7*1)+(6*9)+(5*7)+(4*4)+(3*1)+(2*0)+(1*6)=154
154 % 10 = 4
So 1319741-06-4 is a valid CAS Registry Number.

1319741-06-4Upstream product

1319741-06-4Downstream Products

212513-29-6 C₃₀H₃₂O₇

1319741-06-4Relevant academic research and scientific papers

Efficient synthesis of dissymmetric malonic acid S, O -esters via monoalcoholysis of symmetric dithiomalonates under neutral conditions

Matsuo, Kazumasa,Shindo, Mitsuru

, p. 4406 - 4409 (2011/10/08)

A novel method for the highly selective synthesis of dissymmetric S,O-malonates starting from symmetric diphenyl dithiomalonates under neutral conditions is described. The key step is the thermal formation of an acylketene, the stability of which would co

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