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TERT-BUTYL 9H-PURIN-6-YLCARBAMATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 309947-88-4 Structure
  • Basic information

    1. Product Name: TERT-BUTYL 9H-PURIN-6-YLCARBAMATE
    2. Synonyms: TERT-BUTYL 9H-PURIN-6-YLCARBAMATE
    3. CAS NO:309947-88-4
    4. Molecular Formula: C10H13N5O2
    5. Molecular Weight: 235.24
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 309947-88-4.mol
  • Chemical Properties

    1. Melting Point: 280-282 °C
    2. Boiling Point: 425.3±25.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.379±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 8.96±0.43(Predicted)
    10. CAS DataBase Reference: TERT-BUTYL 9H-PURIN-6-YLCARBAMATE(CAS DataBase Reference)
    11. NIST Chemistry Reference: TERT-BUTYL 9H-PURIN-6-YLCARBAMATE(309947-88-4)
    12. EPA Substance Registry System: TERT-BUTYL 9H-PURIN-6-YLCARBAMATE(309947-88-4)
  • 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: 309947-88-4(Hazardous Substances Data)

309947-88-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 309947-88-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,9,9,4 and 7 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 309947-88:
(8*3)+(7*0)+(6*9)+(5*9)+(4*4)+(3*7)+(2*8)+(1*8)=184
184 % 10 = 4
So 309947-88-4 is a valid CAS Registry Number.

309947-88-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl N-(7H-purin-6-yl)carbamate

1.2 Other means of identification

Product number -
Other names TERT-BUTYL 9H-PURIN-6-YLCARBAMATE

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:309947-88-4 SDS

309947-88-4Relevant articles and documents

LIPID COMPOUNDS AND LIPID NANOPARTICLE COMPOSITIONS

-

Paragraph 00343, (2022/03/02)

Provided herein are lipid compounds that can be used in combination with other lipid components, such as neutral lipids, cholesterol and polymer conjugated lipids, to form lipid nanoparticles for delivery of therapeutic agents (e.g., nucleic acid molecules) for therapeutic or prophylactic purposes, including vaccination. Also provided herein are lipid nanoparticle compositions comprising said lipid compounds.

Selection of new sequence-selective unnatural peptides binding to double-stranded deoxyribonucleic acids (dsDNA) by means of a gel-retardation experiment for library analysis

Chaltin, Patrick,Lescrinier, Eveline,Lescrinier, Theo,Rozenski, Jef,Hendrix, Chris,Rosemeyer, Helmut,Busson, Roger,Van Aerschot, Arthur,Herdewijn, Piet

, p. 2258 - 2283 (2007/10/03)

Previously, we developed a methodology for the solid-phase screening of peptide libraries for interaction with double-stranded deoxyribonucleic acids (dsDNA). In the search for new and more-potent DNA ligands, we investigated the strategy of solution-phas

Synthesis of nucleic-acid base containing norbornene derivatives as monomers for ring-opening-metathesis-polymerization

Davies, R. Gareth,Gibson, Vernon C.,Hursthouse, Michael B.,Light, Mark E.,Marshall, Edward L.,North, Michael,Robson, David A.,Thompson, Ian,White, Andrew J. P.,Williams, David J.,Williams, Paul J.

, p. 3365 - 3381 (2007/10/03)

A series of norbornene derivatives containing nucleic-acid bases (thymine, adenine, cytosine, guanine, or uracil) have been prepared as monomers for ring-opening-metathesis-polymerization (ROMP). Many of the initially prepared monomers had poor solubility but this could be overcome by appropriate choice of a linker between the norbornene and base units. Some of the monomers were successfully polymerised to give homopolymers derived from nucleic-acid base.

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