Cas 112766-25-3,Hydrazinecarboxylic acid, 2-[2-ethoxy-1-(4-methoxyphenyl)-2-oxoethyl]-, methyl ester

112766-25-3

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Basic information

Product Name: Hydrazinecarboxylic acid, 2-[2-ethoxy-1-(4-methoxyphenyl)-2-oxoethyl]-, methyl ester
Synonyms:
CAS NO:112766-25-3
Molecular Formula: C13H18N2O5
Molecular Weight: 282.296
EINECS: N/A
Product Categories: N/A
Mol File: 112766-25-3.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: Hydrazinecarboxylic acid, 2-[2-ethoxy-1-(4-methoxyphenyl)-2-oxoethyl]-, methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Hydrazinecarboxylic acid, 2-[2-ethoxy-1-(4-methoxyphenyl)-2-oxoethyl]-, methyl ester(112766-25-3)
EPA Substance Registry System: Hydrazinecarboxylic acid, 2-[2-ethoxy-1-(4-methoxyphenyl)-2-oxoethyl]-, methyl ester(112766-25-3)

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: 112766-25-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 112766-25-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,7,6 and 6 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 112766-25:
(8*1)+(7*1)+(6*2)+(5*7)+(4*6)+(3*6)+(2*2)+(1*5)=113
113 % 10 = 3
So 112766-25-3 is a valid CAS Registry Number.

112766-25-3Upstream product

112766-25-3Downstream Products

107986-90-3 Ethyl α-<3-(5-Methoxy-1,3,4-oxadiazol-2-onyl)>(p-methoxyphenyl)acetate

112766-25-3Relevant articles and documents

Synthesis of 1,3,4-Oxadiazol-2-ones with Aliphatic Groups at N-3

Huang, Jamin,Bushey, Dean F.,Graves, Michael D.,Johnson, Brenda F.,Singleton, Dianne D.

, p. 1 - 7 (2007/10/02)

A series of 3-substituted-5-methoxy-1,3,4-oxadiazol-2-ones were prepared from aldehydes, ketones, phenylacetic acids, and 1,2- and 1,3-diketones.Conditions for the formation of these oxadiazolones from the precursor N-carbamoyl chlorides depended on the s

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