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N-(1-cyclopropylethylideneamino)-4-methyl-benzenesulfonamide is a chemical compound with the molecular formula C12H16N2O2S. It is an organic molecule that features a benzene ring with a sulfonamide group attached to the para position (the fourth carbon). The sulfonamide group is connected to a cyclopropylethylideneamine moiety, which consists of a cyclopropane ring and an ethylenediamine chain. N-(1-cyclopropylethylideneamino)-4-methyl-benzenesulfonamide is known for its potential pharmaceutical applications, particularly as an antimicrobial agent. It is structurally related to sulfonamide drugs, which are a class of antibiotics that inhibit bacterial growth by interfering with folic acid synthesis in bacteria. The specific arrangement of atoms in N-(1-cyclopropylethylideneamino)-4-methyl-benzenesulfonamide may confer unique properties or activities, making it a subject of interest in the field of medicinal chemistry.

5508-41-8

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5508-41-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5508-41-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,0 and 8 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5508-41:
(6*5)+(5*5)+(4*0)+(3*8)+(2*4)+(1*1)=88
88 % 10 = 8
So 5508-41-8 is a valid CAS Registry Number.

5508-41-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(1-cyclopropylethylideneamino)-4-methylbenzenesulfonamide

1.2 Other means of identification

Product number -
Other names cyclopropanecarboxylic acid methyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5508-41-8 SDS

5508-41-8Relevant academic research and scientific papers

Conformational stability from variable temperature infrared spectra of krypton and xenon solutions, ab initio calculations, vibrational assignment and r0 structural parameters of vinylcyclopropane

Durig, James R.,Zheng, Chao,Deeb, Hamondeh,Guirgis, Gamil A.

, p. 3 - 17 (2005)

The infrared spectra (3200-400 cm-1) of krypton and xenon solutions of vinylcyclopropane c-C3H5CHCH2, at variable temperatures (-55 to -150°C) have been recorded. Additionally, the infrared spectra (3200-250 cm

A simple synthesis of 1-methylcyclobutene

Person, Abigail L.,Thamattoor, Dasan M.

, p. 2973 - 2978 (1999)

Controlled thermal decomposition of the sodium salt of cyclopropyl methyl ketone tosylhydrazone gives 1-methylcyclobutene of excellent purity in good yield.

Preparation method of 1-(4-chlorphenyl)-2-cyclopropyl-1-actone

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Paragraph 0032-0034, (2018/04/03)

The invention provides a preparation method of 1-(4-chlorphenyl)-2-cyclopropyl-1-actone. The 1-(4-chlorphenyl)-2-cyclopropyl-1-actone is prepared by reacting a compound of a structure in Formula (II)with p-chlorobenzaldehyde. The reaction raw material is low in price and easy to obtain, and the production cost is greatly reduced; the synthetic route is short and simple in technique; the raw material preparation and synthesis of the 1-(4-chlorphenyl)-2-cyclopropyl-1-actone are free from waste water, thus the risk to people and environment is reduced; and the green and environment-friendly chemical industry development requirement is met.

Experimental evidence of a cyclopropylcarbinyl conjugative electronic effect

Leber, Phyllis A.,Nocket, Anthony J.,Wipperman, Matthew F.,Zohrabian, Sylvia,Bemis, Christopher Y.,Sidhu, Munsha K.

supporting information, p. 5994 - 5997 (2013/09/12)

Bicyclo[3.2.0]hept-2-enes undergo thermal rearrangement to norbornenes via diradical transition structures. The synthesis of exo-7-cyclopropylbicyclo[3.2. 0]hept-2-ene has been achieved by cycloaddition of cyclopentadiene and cyclopropylketene, generated by treatment of cyclopropylacetyl chloride with triethylamine. A comparison of the cyclopropyl substituent effect with that of other C7 substituents provides experimental evidence of an electron-donating conjugative effect on the transient diradical transition structure in the thermal reaction of exo-7-cyclopropylbicyclo[3.2.0]hept-2-ene. The Royal Society of Chemistry.

Palladium-catalyzed cross-coupling of cyclopropylmethyl N-tosylhydrazones with aromatic bromides: An easy access to multisubstituted 1,3-butadienes

Yang, Qin,Chai, Huining,Liu, Tingting,Yu, Zhengkun

supporting information, p. 6485 - 6489 (2013/11/19)

Direct synthesis of 1,1-disubstitued 1,3-butadienes has been efficiently realized from the cross-coupling of cyclopropylmethyl N-tosylhydrazones with aromatic bromides by means of PdCl2(MeCN)2 as catalyst. 1,1,4-Trisubstitued 1,3-but

Fourier transform rotational spectrum and molecular structure of vinylcyclopropane

Kisiel,Fowler,Legon,Dixneuf

, p. 907 - 911 (2007/10/03)

The sensitive method of pulsed-nozzle Fourier-transform microwave spectroscopy has been employed to record selected weaker features of the natural abundance rotational spectrum of vinylcyclopropane. The weak μc type rotational transitions of th

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