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Thymidine, 3'-O-[bis(4-methoxyphenyl)phenylmethyl]-, 5'-acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 76054-82-5 Structure
  • Basic information

    1. Product Name: Thymidine, 3'-O-[bis(4-methoxyphenyl)phenylmethyl]-, 5'-acetate
    2. Synonyms:
    3. CAS NO:76054-82-5
    4. Molecular Formula: C33H34N2O8
    5. Molecular Weight: 586.642
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 76054-82-5.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: Thymidine, 3'-O-[bis(4-methoxyphenyl)phenylmethyl]-, 5'-acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: Thymidine, 3'-O-[bis(4-methoxyphenyl)phenylmethyl]-, 5'-acetate(76054-82-5)
    11. EPA Substance Registry System: Thymidine, 3'-O-[bis(4-methoxyphenyl)phenylmethyl]-, 5'-acetate(76054-82-5)
  • 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: 76054-82-5(Hazardous Substances Data)

76054-82-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76054-82-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,0,5 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 76054-82:
(7*7)+(6*6)+(5*0)+(4*5)+(3*4)+(2*8)+(1*2)=135
135 % 10 = 5
So 76054-82-5 is a valid CAS Registry Number.

76054-82-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [(2R,3S,5R)-3-[bis(4-methoxyphenyl)-phenylmethoxy]-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methyl acetate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:76054-82-5 SDS

76054-82-5Relevant articles and documents

Synthesis of covalently linked parallel and antiparallel DNA duplexes containing the metal-mediated base pairs T-Hg(ii)-T and C-Ag(i)-C

Ono, Takashi,Yoshida, Kyohei,Saotome, Yuko,Sakabe, Rei,Okamoto, Itaru,Ono, Akira

supporting information; experimental part, p. 1542 - 1544 (2011/03/22)

DNA duplexes fixed in anti-parallel and parallel orientations by introducing covalent linkages have been synthesized and metal ions, Hg(ii) and Ag(i), were incorporated into pyrimidine-pyrimidine base pairs.

3'-O-FORMYL-(N-ACYL)-2'-DEOXYRIBONUCLEOSIDES AS BUILDING UNITS IN THE SYNTHESIS OF OLIGODEOXYRIBONUCLEOTIDES

Smrt, Jiri

, p. 2157 - 2169 (2007/10/02)

5'-O-Dimethoxytrityl-(N-acyl)-2'-deoxyribonucleosides afford 3'-O-formyl-(N-acyl)-2'-deoxyribonucleosides Ia-Id by the action of formic acetic anhydride followed by the action of 80percent aqueous acetic acid.The formyl group is removed from Ia-Id by treatment with 1 mol l-1 triethylamine. 3'-O-Formyl-2'-deoxythymidine (Ia) gives 3'-O-dimethoxytrityl-2'-deoxythymidine (V) by subsequent treatment with acetic anhydride, triethylamine, dimethoxytrityl chloride and methanolic ammonia.The use of compounds I for the synthesis of d-GGAGG (XIX) and d-T16 (XXXII) is described.Systems for thin-layer chromatography of 5'-O-dimethyltrityl-oligodeoxyribonucleotides on silica gel are described.

THE USE OF ZINC BROMIDE FOR REMOVAL OF DIMETHOXYTRITYL ETHERS FROM DEOXYNUCLEOSIDES

Matteucci, M. D.,Caruthers, M. H.

, p. 3243 - 3246 (2007/10/02)

Zinc bromide has been observed to detritylate specifically 5'-trityldeoxy-deoxynucleosides whereas 3'-trityl ethers are not cleaved.Of additional practical consideration and in contrast to protic acids, no depurination was observed with this reagent.

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