Cas 1174231-77-6,ethyl 4-allyl-5-(phenylthio)-1-(2-trimethylsilylethoxymethyl)-1H-pyrazole-3-carboxylate

1174231-77-6

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Basic information

Product Name: ethyl 4-allyl-5-(phenylthio)-1-(2-trimethylsilylethoxymethyl)-1H-pyrazole-3-carboxylate
Synonyms: ethyl 4-allyl-5-(phenylthio)-1-(2-trimethylsilylethoxymethyl)-1H-pyrazole-3-carboxylate
CAS NO:1174231-77-6
Molecular Formula:
Molecular Weight: 418.632
EINECS: N/A
Product Categories: N/A
Mol File: 1174231-77-6.mol
Article Data: 1

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: ethyl 4-allyl-5-(phenylthio)-1-(2-trimethylsilylethoxymethyl)-1H-pyrazole-3-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 4-allyl-5-(phenylthio)-1-(2-trimethylsilylethoxymethyl)-1H-pyrazole-3-carboxylate(1174231-77-6)
EPA Substance Registry System: ethyl 4-allyl-5-(phenylthio)-1-(2-trimethylsilylethoxymethyl)-1H-pyrazole-3-carboxylate(1174231-77-6)

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: 1174231-77-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1174231-77-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,4,2,3 and 1 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1174231-77:
(9*1)+(8*1)+(7*7)+(6*4)+(5*2)+(4*3)+(3*1)+(2*7)+(1*7)=136
136 % 10 = 6
So 1174231-77-6 is a valid CAS Registry Number.

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1174231-77-6Relevant articles and documents

Synthesis of fully substituted pyrazoles via regio- and chemoselective metalations

Despotopoulou, Christina,Klier, Lydia,Knochel, Paul

, p. 3326 - 3329 (2009)

The full functionalization of the pyrazole ring was achieved by successive regioselective metalations using TMPMgCI-LiCI and TMP2Mg.2LiCI. Trapping with various electrophiles led to trisubstituted pyrazoles. An application to the synthesis of the acaricide Tebufenpyrad is reported.

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