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N-Acetylsulfanilyl chloride

Name: <I>N</I>-Acetylsulfanilyl chloride
Brand: ALDRICH

98%

Synonym(s):

4-Acetamidobenzenesulfonyl chloride

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About This Item

Linear Formula:

4-(CH₃CONH)C₆H₄SO₂Cl

CAS Number:

121-60-8

Molecular Weight:

233.67

Beilstein:

746676

EC Number:

204-485-1

MDL number:

MFCD00007442

UNSPSC Code:

12352100

PubChem Substance ID:

24847112

NACRES:

NA.22

Assay

98%

mp

142-145 °C (dec.) (lit.)

SMILES string

CC(=O)Nc1ccc(cc1)S(Cl)(=O)=O

InChI

1S/C8H8ClNO3S/c1-6(11)10-7-2-4-8(5-3-7)14(9,12)13/h2-5H,1H3,(H,10,11)

InChI key

GRDXCFKBQWDAJH-UHFFFAOYSA-N

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Organic Building Blocks

General description

L-hydroxyproline has been derivatized with N-acetylsulfanilyl chloride and 5-chlorovaleric acid during the synthesis of the haptens HP1 and HP2.

Application

N-Acetylsulfanilyl chloride is used in the synthesis of N1,N1-dimethylsulfanilamide as the internal standard in the reaction. The reaction is used to determine tramadol and its O-desmethylated metabolite in blood plasma.

Pictograms

GHS05,GHS07

Signal Word

Danger

Hazard Statements

H314,H335

Precautionary Statements

P260 - P271 - P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338

Hazard Classifications

Skin Corr. 1B - STOT SE 3

Target Organs

Respiratory system

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Synthesis of hapten and production of a monoclonal antibody against a derivative of L-hydroxyproline, a special amino acid in hydrolyzed animal protein.

Li L Wang et al.

Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 48(1), 9-15 (2012-10-04)

China's government has prohibited the addition of simply hydrolyzed animal protein from solid leather waste into milk. The objective of this study was to produce a monoclonal antibody against L-hydroxyproline, a special amino acid in hydrolyzed animal protein. L-hydroxyproline was

N-phenylsulfonyl-3,5-bis(arylidene)-4-piperidone derivatives as activation NF-κB inhibitors in hepatic carcinoma cell lines.

Ning Li et al.

European journal of medicinal chemistry, 155, 531-544 (2018-06-18)

Ten novel symmetric 3,5-bis(arylidene)-4-piperidone derivatives (BAPs, 1-10) and fourteen dissymmetric BAPs (11-24) were synthesized and evaluated the cytotoxicity. All of the compounds have been screened for their anti-inflammatory activity characterized by evaluating their inhibitory effects on LPS-induced IL-6, TNF-α secretion.

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