Cas 116307-63-2,Acetic acid, [2,3-dichloro-4-[[1-(ethoxymethyl)-1H-pyrazol-5-yl]carbonyl]phenoxy]-, ethyl ester

116307-63-2

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Basic information

Product Name: Acetic acid, [2,3-dichloro-4-[[1-(ethoxymethyl)-1H-pyrazol-5-yl]carbonyl]phenoxy]-, ethyl ester
Synonyms:
CAS NO:116307-63-2
Molecular Formula: C17H18Cl2N2O5
Molecular Weight: 401.246
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, [2,3-dichloro-4-[[1-(ethoxymethyl)-1H-pyrazol-5-yl]carbonyl]phenoxy]-, ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid, [2,3-dichloro-4-[[1-(ethoxymethyl)-1H-pyrazol-5-yl]carbonyl]phenoxy]-, ethyl ester(116307-63-2)
EPA Substance Registry System: Acetic acid, [2,3-dichloro-4-[[1-(ethoxymethyl)-1H-pyrazol-5-yl]carbonyl]phenoxy]-, ethyl ester(116307-63-2)

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: 116307-63-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 116307-63-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,3,0 and 7 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 116307-63:
(8*1)+(7*1)+(6*6)+(5*3)+(4*0)+(3*7)+(2*6)+(1*3)=102
102 % 10 = 2
So 116307-63-2 is a valid CAS Registry Number.

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116307-63-2Relevant academic research and scientific papers

Phenoxyacetic acid derivatives composition and use

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, (2008/06/13)

Novel phenoxyacetic acid derivatives of the formula: STR1 wherein A is a substituted or unsubstituted 5-pyrazolyl group, R1 is hydrogen atom or a lower alkyl group, R2 is hydrogen atom or a lower alkenyl group, X is a halogen atom and Z is oxygen atom or methylene group, and salts thereof have potent diuretic, saluretic and uricosuric activities.

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