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3-chloro-4-hydroxyphenylacetic acid 2,4,5-trichlorophenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 199930-20-6 Structure
  • Basic information

    1. Product Name: 3-chloro-4-hydroxyphenylacetic acid 2,4,5-trichlorophenyl ester
    2. Synonyms:
    3. CAS NO:199930-20-6
    4. Molecular Formula:
    5. Molecular Weight: 366.028
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 199930-20-6.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: 3-chloro-4-hydroxyphenylacetic acid 2,4,5-trichlorophenyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-chloro-4-hydroxyphenylacetic acid 2,4,5-trichlorophenyl ester(199930-20-6)
    11. EPA Substance Registry System: 3-chloro-4-hydroxyphenylacetic acid 2,4,5-trichlorophenyl ester(199930-20-6)
  • 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: 199930-20-6(Hazardous Substances Data)

199930-20-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 199930-20-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,9,9,3 and 0 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 199930-20:
(8*1)+(7*9)+(6*9)+(5*9)+(4*3)+(3*0)+(2*2)+(1*0)=186
186 % 10 = 6
So 199930-20-6 is a valid CAS Registry Number.

199930-20-6Downstream Products

199930-20-6Relevant articles and documents

General process for the preparation of cyclic oligonucleotides

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, (2008/06/13)

The preparation process starts with a protected nucleotide which is anchored through its phosphate group with an anchoring group that links the phosphate group to a polymeric support, its 5'-hydroxyl group is protected for chain elongation and its 3'-terminal phosphate group is protected with a chain phosphate protecting group. Elongation is carried out under conditions in which the protecting groups of adenine, cytosine and guanine remain unaltered and thymine and uracil groups are not protected. Chain phosphate protecting groups are removed from the obtained cyclic anchored intermediate. Then the product is cleaved from the polymeric support and the protecting groups of the nucleobases are removed. The process has the advantages of general utility for any bases and any size of cycle and of providing high yields with minor by-products. The cyclic oligonucleotides obtained have potential use as antisense products and probes, as well as in therapeutics and in diagnosis.

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