Cas 107300-85-6,N-(2-(3,4-DIMETHOXYPHENYL)ETHYL)-2-(4-METHYL(3,2,5-OXADIAZOLYL))ETHANAMIDE

107300-85-6

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Basic information

Product Name: N-(2-(3,4-DIMETHOXYPHENYL)ETHYL)-2-(4-METHYL(3,2,5-OXADIAZOLYL))ETHANAMIDE
Synonyms: N-(2-(3,4-DIMETHOXYPHENYL)ETHYL)-2-(4-METHYL(3,2,5-OXADIAZOLYL))ETHANAMIDE;N-[2-(3,4-dimethoxyphenyl)ethyl]-2-(5-methyl-1,2,4-oxadiazol-3-yl)acetamide
CAS NO:107300-85-6
Molecular Formula: C₁₅H₁₉N₃O₄
Molecular Weight: 305.33
EINECS: N/A
Product Categories: N/A
Mol File: 107300-85-6.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: N-(2-(3,4-DIMETHOXYPHENYL)ETHYL)-2-(4-METHYL(3,2,5-OXADIAZOLYL))ETHANAMIDE(CAS DataBase Reference)
NIST Chemistry Reference: N-(2-(3,4-DIMETHOXYPHENYL)ETHYL)-2-(4-METHYL(3,2,5-OXADIAZOLYL))ETHANAMIDE(107300-85-6)
EPA Substance Registry System: N-(2-(3,4-DIMETHOXYPHENYL)ETHYL)-2-(4-METHYL(3,2,5-OXADIAZOLYL))ETHANAMIDE(107300-85-6)

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: 107300-85-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 107300-85-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,3,0 and 0 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 107300-85:
(8*1)+(7*0)+(6*7)+(5*3)+(4*0)+(3*0)+(2*8)+(1*5)=86
86 % 10 = 6
So 107300-85-6 is a valid CAS Registry Number.

107300-85-6Upstream product

107300-85-6Downstream Products

107300-85-6Relevant articles and documents

Synthesis of 4-Aminopyrimidines from 1,2,4-Oxadiazoles, II A General Method for the Preparation of 4-Substituted 6,7-Dihydro-9,10-dialkoxy-2H-pyrimidoisoquinolin-2-imine Hydrochlorides

Korbonits, Dezsoe,Kiss, Pal,Bata, Imre,Heja, Gergely,Simon, Kalman,Kolonits, Pal

, p. 1039 - 1044 (2007/10/02)

5'-Substituted 1--3,4-dihydroisoquinolines (7) were reduced by NaBH4 selectively to give the corresponding tetrahydroisoquinolines (8) which underwent ring isomerization to pyrazoloisoquinolines (9).Catalytic hydrogena

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