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269670

4-tert-Butylbenzenesulfonyl chloride

Name: 4-<I>tert</I>-Butylbenzenesulfonyl chloride
Brand: ALDRICH

98%

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About This Item

Linear Formula:

(CH₃)₃CC₆H₄SO₂Cl

CAS Number:

15084-51-2

Molecular Weight:

232.73

NACRES:

NA.22

PubChem Substance ID:

24856338

UNSPSC Code:

12352100

MDL number:

MFCD00007449

Assay:

98%

Form:

solid

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Properties

Quality Level

100

assay

98%

form

solid

mp

78-81 °C (lit.)

SMILES string

CC(C)(C)c1ccc(cc1)S(Cl)(=O)=O

InChI

1S/C10H13ClO2S/c1-10(2,3)8-4-6-9(7-5-8)14(11,12)13/h4-7H,1-3H3

InChI key

YEZADZMMVHWFIY-UHFFFAOYSA-N

Description

Application

4-tert-Butylbenzenesulfonyl chloride was used in the synthesis of 1-[bis-(4-fluorophenyl)-methyl]-4-(4-tert-butylbenzenesulfonyl)piperazine.

pictograms

GHS05

signalword

Danger

hcodes

H314

pcodes

P260 - P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338 - P363

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Regulatory Information

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Synthesis and in vitro antimicrobial studies of medicinally important novel N-alkyl and N-sulfonyl derivatives of 1-[bis(4-fluorophenyl)-methyl]piperazine.

J N Narendra Sharath Chandra et al.

Bioorganic & medicinal chemistry, 14(19), 6621-6627 (2006-06-21)

A series of novel substituted 1-[bis(4-fluorophenyl)-methyl]piperazine derivatives (4a-g) and (5h-m) have been synthesized. The synthesized compounds were characterized by IR and 1H NMR. All the synthesized compounds were evaluated in vitro for their efficacy as antimicrobial agents against representative strains

Global Trade Item Number

SKU	GTIN
269670-50G	04061826141588
269670-10G	04061826141571