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144364-01-2

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144364-01-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144364-01-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,3,6 and 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 144364-01:
(8*1)+(7*4)+(6*4)+(5*3)+(4*6)+(3*4)+(2*0)+(1*1)=112
112 % 10 = 2
So 144364-01-2 is a valid CAS Registry Number.

144364-01-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-chloro-9-prop-2-enylpurin-2-amine

1.2 Other means of identification

Product number -
Other names N9-allyl-2-amino-6-chloropurine

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:144364-01-2 SDS

144364-01-2Relevant articles and documents

Guanine-copper coordination polymers: Crystal analysis and application as thin film precursors

Nagapradeep,Venkatesh,Tripathi,Verma, Sandeep

, p. 1744 - 1752 (2014)

Three copper-N9-modified guanine complexes are reported with structures ranging from a discrete trinuclear motif to a mixed-valence coordination polymer. These complexes were used as precursors for the deposition and growth of copper oxide thin films on Si(100), at two different annealing temperatures, by using a CVD technique. Subsequent resistivity measurements suggest the formation of conductive thin films, raising the possibility of using nucleobase-metal complexes as versatile thin film precursors. The Royal Society of Chemistry.

Synthesis of silicon analogues of acyclonucleotides incorporable in oligonucleotide solid-phase synthesis

Thibon, Jacques,Latxague, Laurent,Deleris, Gerard

, p. 4635 - 4642 (2007/10/03)

The synthesis of the four silicon analogues of acyclonucleosides was described. In every case, the silicon atom was introduced onto an allyl group on the natural nucleobase following a hydrosilylation reaction. Diols obtained were protected as 4,4'-dimethoxytrityl ethers and subsequently activated as 2-cyanoethyl N,N-diisopropylchlorophosphoramidite in order to be suitable for oligonucleotide solid phase synthesis.

Fmoc Mediated Synthesis of Peptide Nucleic Acids.

Thomson, Stephen A.,Josey, John A.,Cadilla, Rodolfo,Gaul, Micheal D.,Hassman, C. Fred,et al.

, p. 6179 - 6194 (2007/10/02)

The syntheses of the Fmoc-protected Peptide Nucleic Acid (PNA) monomer pentafluorophenyl esters of adenine (26), cytosine (23), guanine (29) and thymine (20), and their oligomerization are described.The Fmoc PNA backbone 1 is prepared as a stable hydrochl

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