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N-[(dimethylamino)methylidene]-9-[2,3-O-(1-methylethylidene)pentofuranosyl]-9H-purin-6-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

29706-75-0

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29706-75-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29706-75-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,7,0 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 29706-75:
(7*2)+(6*9)+(5*7)+(4*0)+(3*6)+(2*7)+(1*5)=140
140 % 10 = 0
So 29706-75-0 is a valid CAS Registry Number.

29706-75-0SDS

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 N'-[9-[6-(hydroxymethyl)-2,2-dimethyl-3a,4,6,6a-tetrahydrofuro[3,4-d][1,3]dioxol-4-yl]purin-6-yl]-N,N-dimethylmethanimidamide

1.2 Other means of identification

Product number -
Other names N6-dimethylaminomethylene-O2',O3'-isopropylidene-adenosine

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:29706-75-0 SDS

29706-75-0Downstream Products

29706-75-0Relevant academic research and scientific papers

INHIBITORS OF ADENYLATE-FORMING ENZYME MENE

-

Paragraph 0428, (2020/08/22)

Provided herein are compounds of Formula (I) and pharmaceutically acceptable salts or tautomers thereof which may inhibit adenylate-forming enzymes. Also provided are pharmaceutical compositions, kits, uses, and methods involving the inventive compounds for the treatment and/or prevention of an infectious disease (e.g., bacterial infection (e.g., tuberculosis, methicillin- resistant Staphylococcus aureus)).

Phosphonoacetic acid derivatives of nucleosides

-

, (2008/06/13)

Phosphonoacetic acid derivatives of purine and pyrimidine nucleosides are novel antiviral and/or antineoplastic agents.

Analogues of S adenosylhomocysteine as potential inhibitors of biological transmethylation. Synthesis of analogues with modifications at the 5' thioether linkage

Chang,Coward

, p. 684 - 691 (2007/10/06)

The synthesis of S adenosylhomocysteine analogues, in which the 5' thioether linkage is replaced by an oxygen or nitrogen isostere, has been investigated. These compounds were designed to be resistant to enzyme catalyzed hydrolytic cleavage of the 5' subs

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