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2-(tert-butylsulfamoyl-methyl)-benzoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 415916-12-0 Structure
  • Basic information

    1. Product Name: 2-(tert-butylsulfamoyl-methyl)-benzoic acid
    2. Synonyms:
    3. CAS NO:415916-12-0
    4. Molecular Formula:
    5. Molecular Weight: 271.337
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 415916-12-0.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: 2-(tert-butylsulfamoyl-methyl)-benzoic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(tert-butylsulfamoyl-methyl)-benzoic acid(415916-12-0)
    11. EPA Substance Registry System: 2-(tert-butylsulfamoyl-methyl)-benzoic acid(415916-12-0)
  • 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: 415916-12-0(Hazardous Substances Data)

415916-12-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 415916-12-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,1,5,9,1 and 6 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 415916-12:
(8*4)+(7*1)+(6*5)+(5*9)+(4*1)+(3*6)+(2*1)+(1*2)=140
140 % 10 = 0
So 415916-12-0 is a valid CAS Registry Number.

415916-12-0Relevant articles and documents

Development of an immunoassay for the residues of the herbicide bensulfuron-methyl.

Lee, Jae Koo,Ahn, Ki Chang,Park, Oee Sook,Ko, Yong Kwan,Kim, Dae-Whang

, p. 1791 - 1803 (2002)

To develop a competitive indirect enzyme-linked immunosorbent assay based on polyclonal antibodies for the detection of the sulfonylurea herbicide bensulfuron-methyl, seven structurally related haptens were synthesized. Four of them mimicking the target analyte were conjugated to keyhole limpet hemocyanin by the N-hydroxysuccinimide activated ester method to use as immunogens, and all of them were conjugated to bovine serum albumin to use as plate-coating antigens. Polyclonal antibodies raised in rabbits and the coating antigens were screened and selected for the assay in simple homologous and heterologous ELISA formats. Three sensitive heterologous ELISAs were selected and optimized, showing the average IC(50) values of bensulfuron-methyl as low as 0.17, 0.09, and 0.09 ng/mL, the detection ranges of 0.04-0.60, 0.01-0.60, and 0.04-0.25 ng/mL, and the lowest detection limits of 0.03, 0.002, and 0.03 ng/mL, respectively. The cross-reactivities of other sulfonylurea herbicides and metabolites of bensulfuron-methyl to the antibodies were less than 15% in the two assays. Recoveries from the analyte-fortified water samples in assay I were in the range of 81-125% by simple dilution. The correlation between the ELISA and HPLC was 0.999 (n = 15) with a slope of 1.37 in the analysis of groundwater samples fortified with bensulfuron-methyl. The results obtained strongly indicate that the ELISA can be a highly sensitive and convenient tool for detecting bensulfuron-methyl residues in agricultural and environmental samples.

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