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Benzenesulfonyl chloride, 4-(phenylthio)-, also known as 4-(phenylthio)benzenesulfonyl chloride or 4-phenylsulfanylbenzenesulfonyl chloride, is an organic compound with the chemical formula C12H9ClO2S2. It is a colorless to pale yellow crystalline solid that is soluble in organic solvents. Benzenesulfonyl chloride, 4-(phenylthio)- is primarily used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. It is also employed as a reagent in various chemical reactions, such as the protection of thiol groups and the formation of sulfonamide bonds. Due to its reactivity, it is essential to handle Benzenesulfonyl chloride, 4-(phenylthio)- with care, as it can cause irritation to the eyes, skin, and respiratory system.

1623-94-5

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1623-94-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1623-94-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,2 and 3 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1623-94:
(6*1)+(5*6)+(4*2)+(3*3)+(2*9)+(1*4)=75
75 % 10 = 5
So 1623-94-5 is a valid CAS Registry Number.

1623-94-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-phenylsulfanylbenzenesulfonyl chloride

1.2 Other means of identification

Product number -
Other names 4-Phenylmercapto-benzolsulfonylchlorid

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:1623-94-5 SDS

1623-94-5Relevant academic research and scientific papers

COMPOUNDS WITH PGD2 ANTAGONIST ACTIVITY

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Page/Page column 82, (2010/02/11)

Compounds of general formula (I); wherein R1, R2, R3 and R4 are independently hydrogen, halo, -C1-C6 alkyl, -O(C1-C6 alkyl), -C1-C6 alkyl(C3-C7 cycloalkyl), -CON(R9)2, -SOR9, -S02R9, -S02N(R9)2, -N(R9)2, -NR9OR9, -C02R9, COR9, -SR9, -OH, -N02 or -CN; each R9 independently hydrogen or C1-C6 alkyl, R5 and R6 are each independently hydrogen, or C1-C6 alkyl or together with the carbon atom to which they are attached form a C3-C7 cycloalkyl group; R7 is hydrogen or C1-C6 alkyl; R8 is C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl or an aromatic moiety, any of which may optionally be substituted with one or more substituents selected from halo, -SOR13 -S02R13, -R14, -OR14, -CON(R14)2 -SOR14, -S02R14, -S02N(R14) -S02N(R14)2, -N(R 14)2, NR14COR14, -CO2R14, COR14, -SR14, -N02 or -CN; wherein R13 is a 5 to 7 membered heterocyclic ring, and each R14 is independently hydrogen, alkyl or aryl, the aryl being optionally substituted by -R9, -OR9, -CON(R9)2, -SOR9 -S02R9, -S02N(R9)2, -N(R9)2, NR9COR9, -C02R9, -COR9, -SR9, halo, -N02 or -CN, wherein R9 is as defined above; provided that when R1, R3 and R4 are hydrogen and R2 is hydrogen, halogen or -0(C1-C6)alkyl, R8 is not unsubstituted phenyl or phenyl substituted by halo, C1-C6 alkyl, -0(C1-C6)alkyl, -S(C1-C6)alkyl or -CO(C1-C6)alkyl, or pharmaceutically acceptable salts, hydrates, solvates, complexes or prodrugs therof are useful in the treatment of allergic diseases such as asthma, allergic rhinitis and atopic dermatitis

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