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4-Amino-2,5-dichlorbenzolsulfochlorid, also known as 4-amino-2,5-dichlorobenzenesulfonyl chloride, is an organic compound with the chemical formula C6H4Cl3NO2S. It is a white to off-white crystalline solid that is soluble in organic solvents. 4-Amino-2,5-dichlorbenzolsulfochlorid is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is also known for its reactivity, as it can undergo nucleophilic substitution reactions with amines, alcohols, and other nucleophiles, making it a valuable building block in organic chemistry. Due to its reactivity and potential hazards, it is important to handle 4-amino-2,5-dichlorbenzolsulfochlorid with care, following proper safety protocols.

4857-94-7

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4857-94-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4857-94-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,5 and 7 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4857-94:
(6*4)+(5*8)+(4*5)+(3*7)+(2*9)+(1*4)=127
127 % 10 = 7
So 4857-94-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H4Cl3NO2S/c7-3-2-6(13(9,11)12)4(8)1-5(3)10/h1-2H,10H2

4857-94-7Relevant academic research and scientific papers

Monoazo dyes which are free from water-solubilizing groups and which contain a fluorosulphonyl group and process for colouring polyamides and polyester materials therewith

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, (2008/06/13)

A process for coloring a synthetic textile material or fibre blend thereof which comprises applying to the synthetic textile material a compound or mixture thereof, which is free from water solubilizing groups, of Formula (1): wherein A and D each independently is an optionally substituted heterocyclic or carbocyclic group and at least one of A or D carries directly at least one --SO2 F group or carries a substituent to which at least one --SO2 F group is attached except for 4-(4-fluorosulphonylphenylazo)-N,N-dimethylaniline, provided that one of A or D is not 3,5-difluorosulphonylthien-2-yl, optionally substituted 1-phenyl-pyrazol-4-yl-5-one or STR1 or that one of A or D does not carry an --NCH2 CH(OH)CH2 Cl, --NCOCH2 Cl or --NCH2 CH2 SO2 F substituent. The presence of one or more --SO2 F groups in a dye molecule generally improves the properties of that dye and confers surprisingly good wet fastness and light fastness properties.

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