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CAS

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88708-07-0

o-aminobenzenesulfonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 88708-07-0 Structure

  • Basic information

    1. Product Name: o-aminobenzenesulfonate
    2. Synonyms: o-aminobenzenesulfonate
    3. CAS NO:88708-07-0
    4. Molecular Formula:
    5. Molecular Weight: 172.185
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 88708-07-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: o-aminobenzenesulfonate(CAS DataBase Reference)
    10. NIST Chemistry Reference: o-aminobenzenesulfonate(88708-07-0)
    11. EPA Substance Registry System: o-aminobenzenesulfonate(88708-07-0)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 88708-07-0(Hazardous Substances Data)

88708-07-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88708-07-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,7,0 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 88708-07:
(7*8)+(6*8)+(5*7)+(4*0)+(3*8)+(2*0)+(1*7)=170
170 % 10 = 0
So 88708-07-0 is a valid CAS Registry Number.

88708-07-0Upstream product

88708-07-0Downstream Products

88708-07-0Relevant articles and documents

Reaction of Phenylhydroxylamine with Bisulfite. A Possible Model for Amine-Mediated Carcinogenesis

Sternson, L.A.,Dixit, A.S.,Becker, A.R.

, p. 57 - 60 (1983)

Under anaerobic conditions, phenylhydroxylamine reacts with the model nucleophile (bi)sulfite to form aniline, o- and p-aminophenol, and o- and p-aminobenzenesulfonate.Evidence is presented suggesting that all products result from intermediates formed from nucleophilic attack of both bisulfite and sulfite on the arylhydroxylamine with subsequent covalent addition-elimination processes leading to products.Such a scheme offers a possible alternative pathway for describing the mechanism for carcinogenic arylation of nucleic acid residues by arylhydroxylamines not requiring the intermediacy of short-lived free radicals or nitrenium ions.

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