Cas 297150-01-7,N-(5-METHYL-3-ISOXAZOLYL)-2-[(5-METHYL-1,3,4-THIADIAZOL-2-YL)SULFANYL]ACETAMIDE

297150-01-7

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Basic information

Product Name: N-(5-METHYL-3-ISOXAZOLYL)-2-[(5-METHYL-1,3,4-THIADIAZOL-2-YL)SULFANYL]ACETAMIDE
Synonyms: N-(5-METHYL-3-ISOXAZOLYL)-2-[(5-METHYL-1,3,4-THIADIAZOL-2-YL)SULFANYL]ACETAMIDE;N-(5-methyl-1,2-oxazol-3-yl)-2-[(5-methyl-1,3,4-thiadiazol-2-yl)sulfanyl]acetamide
CAS NO:297150-01-7
Molecular Formula: C9H10N4O2S2
Molecular Weight: 270.33
EINECS: N/A
Product Categories: N/A
Mol File: 297150-01-7.mol

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-(5-METHYL-3-ISOXAZOLYL)-2-[(5-METHYL-1,3,4-THIADIAZOL-2-YL)SULFANYL]ACETAMIDE(CAS DataBase Reference)
NIST Chemistry Reference: N-(5-METHYL-3-ISOXAZOLYL)-2-[(5-METHYL-1,3,4-THIADIAZOL-2-YL)SULFANYL]ACETAMIDE(297150-01-7)
EPA Substance Registry System: N-(5-METHYL-3-ISOXAZOLYL)-2-[(5-METHYL-1,3,4-THIADIAZOL-2-YL)SULFANYL]ACETAMIDE(297150-01-7)

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: 297150-01-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 297150-01-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,7,1,5 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 297150-01:
(8*2)+(7*9)+(6*7)+(5*1)+(4*5)+(3*0)+(2*0)+(1*1)=147
147 % 10 = 7
So 297150-01-7 is a valid CAS Registry Number.

297150-01-7Upstream product

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297150-01-7Relevant academic research and scientific papers

Antimicrobial and anticancer effects of some 2-(substitutedsulfanyl)-N-(5- methyl-isoxazol-3-yl)acetamide derivatives

Oezkay, Yusuf,Incesu, Zerrin,Oender, Nur Ipek,TunalI, Yagmur,Karaca, Huelya,IsIkdag, Ilhan,Ucucu, Uemit

, p. 211 - 218 (2013/03/14)

In the present study, some isoxazole-(benz)azole derivatives (3a-3j) were synthesized by considering antimicrobial and anticancer potencies of azole compounds. Chemical structures of obtained compounds (3a-3j) were confirmed by the data of spectral and el

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