Cas 794553-00-7,4-methyl-N-(3-methylphenyl)-N-[1-(3-methylphenyl)-4-oxo-3-phenoxy-2-azetidinyl]benzenesulfonamide

794553-00-7

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Basic information

Product Name: 4-methyl-N-(3-methylphenyl)-N-[1-(3-methylphenyl)-4-oxo-3-phenoxy-2-azetidinyl]benzenesulfonamide
Synonyms: 4-methyl-N-(3-methylphenyl)-N-[1-(3-methylphenyl)-4-oxo-3-phenoxy-2-azetidinyl]benzenesulfonamide
CAS NO:794553-00-7
Molecular Formula: C30H28N2O4S
Molecular Weight: 512.61932
EINECS: N/A
Product Categories: N/A
Mol File: 794553-00-7.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: 4-methyl-N-(3-methylphenyl)-N-[1-(3-methylphenyl)-4-oxo-3-phenoxy-2-azetidinyl]benzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: 4-methyl-N-(3-methylphenyl)-N-[1-(3-methylphenyl)-4-oxo-3-phenoxy-2-azetidinyl]benzenesulfonamide(794553-00-7)
EPA Substance Registry System: 4-methyl-N-(3-methylphenyl)-N-[1-(3-methylphenyl)-4-oxo-3-phenoxy-2-azetidinyl]benzenesulfonamide(794553-00-7)

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: 794553-00-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 794553-00-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,4,5,5 and 3 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 794553-00:
(8*7)+(7*9)+(6*4)+(5*5)+(4*5)+(3*3)+(2*0)+(1*0)=197
197 % 10 = 7
So 794553-00-7 is a valid CAS Registry Number.

794553-00-7Upstream product

794553-00-7Downstream Products

794553-00-7Relevant academic research and scientific papers

Facile synthesis of 4-acylamino and 4-sulphonamido β-lactams

Thiagarajan,Puranik,Deshmukh,Bhawal

, p. 7811 - 7816 (2000)

The cycloaddition reaction of trisubstituted amidines (7a-f) with acid chlorides in presence of triethylamine gave 4-acylamino and 4-sulphonamido-trans-β-lactams (9a-h) in very good yields. Similarly N,N'-diarylamidines (5a-d) on reaction with 2 equiv. of acid chlorides (8a,b) gave 4-acylamino-trans-β-lactams (10a-e) via in situ generated acylamidines followed by cycloaddition reaction. (C) 2000 Elsevier Science Ltd.

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