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(4-acetamido-2,6-dimethylphenyl)sulfinic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 132414-07-4 Structure
  • Basic information

    1. Product Name: (4-acetamido-2,6-dimethylphenyl)sulfinic acid
    2. Synonyms: (4-acetamido-2,6-dimethylphenyl)sulfinic acid
    3. CAS NO:132414-07-4
    4. Molecular Formula:
    5. Molecular Weight: 227.284
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 132414-07-4.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: (4-acetamido-2,6-dimethylphenyl)sulfinic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4-acetamido-2,6-dimethylphenyl)sulfinic acid(132414-07-4)
    11. EPA Substance Registry System: (4-acetamido-2,6-dimethylphenyl)sulfinic acid(132414-07-4)
  • 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: 132414-07-4(Hazardous Substances Data)

132414-07-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132414-07-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,4,1 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 132414-07:
(8*1)+(7*3)+(6*2)+(5*4)+(4*1)+(3*4)+(2*0)+(1*7)=84
84 % 10 = 4
So 132414-07-4 is a valid CAS Registry Number.

132414-07-4Relevant articles and documents

Phenylsulfonylnitromethanes as potent irreversible inhibitors of aldose reductase

Saab, Nada H.,Donkor, Isaac O.,Rodriguez, Libaniel,Kador, Peter F.,Miller, Duane D.

, p. 745 - 751 (2007/10/03)

Aldose reductase (AR) inhibition provides a viable pharmacologically direct mode for the treatment of diabetic complications. We have synthesized a series of N-4 substituted analogues (15-21) of the known aldose reductase inhibitor phenyl-sulfonylnitromethane. The compounds are potent inhibitors of AR with IC50s between 0.01 and 0.19 μM. Some of the compounds are also potent affinity labels for AR. Compound 19 exhibits the highest and almost complete irreversible inhibition of AR known to date.

AMIDOBENZENE DERIVATIVES, COMPOSITIONS AND USE

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, (2008/06/13)

The invention concerns novel phenoxy- and phenylthio-acetyl derivatives of (4-amino-2,6-dimethyl-phenylsulphonyl)nitromethane and pharmaceutically acceptable salts thereof which are inhibitors of the enzyme aldose reductase and are of value, for example,

ACETAMIDE DERIVATIVES

-

, (2008/06/13)

The invention concerns novel N-phenylacetyl and related acyl derivatives of (4-amino-2,6-dimethylphenylsulphonyl)nitromethane and pharmaceutically acceptable salts thereof which are inhibitors of the enzyme aldose reductase and are of value, for example,i

AMIDE DERIVATIVES, COMPOSITIONS AND USE

-

, (2008/06/13)

The invention concerns novel (oxamido- and ureido-phenylsulfonyl)nitromethane derivatives and pharmaceutically acceptable salts thereof which are inhibitors of the enzyme aldose reductase and are of value, for example, in the treatment of certain peripher

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