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3-Pentofuranosylpyrimidine-2,4(1H,3H)-dione, also known as 3-deoxy-D-ribofuranosyl-pyrimidin-2,4-dione, is a chemical compound that plays a significant role in the structure of certain nucleosides. It is a derivative of pyrimidine, a heterocyclic aromatic organic compound consisting of a six-membered ring with four carbon atoms and two nitrogen atoms. The compound is characterized by the presence of a pentofuranosyl group, which is a five-carbon sugar moiety, attached to the pyrimidine ring. This specific arrangement is found in some nucleosides, which are the building blocks of nucleic acids like DNA and RNA. The compound's structure is essential for understanding the chemistry of nucleic acids and their interactions within biological systems.

6745-33-1

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6745-33-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6745-33-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,4 and 5 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6745-33:
(6*6)+(5*7)+(4*4)+(3*5)+(2*3)+(1*3)=111
111 % 10 = 1
So 6745-33-1 is a valid CAS Registry Number.

6745-33-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,11-diamino-2-ethylnaphtho[2,3-f]isoindole-1,3,5,10-tetrone

1.2 Other means of identification

Product number -
Other names [2-(1(2)H-indazol-3-yl)-propyl]-dimethyl-amine

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:6745-33-1 SDS

6745-33-1Downstream Products

6745-33-1Relevant academic research and scientific papers

5-FLUOROURACIL DERIVATES. VII. TERT-AMINE PROMOTED N-GLYCOSIDATION OF OYRIMIDINES

Ozaki, Shoichiro,Watanabe, Yutaka,Hoshiko, Tomori,Fujisawa, Hiroshi,Uemura, Atsuhiko,Ohrai, Kazuhiko

, p. 5061 - 5062 (2007/10/02)

Acylglycosyl halides react smoothly with N1- and N3-(octylthio)-carbonylpyrimidines in the presence of tert-amine to give the corresponding nucleosides in good yields.

A New Synthesis of 3-(β-D-Ribofuranosyl)uracil (Isouridine) via the Intermediacy of a O6,5'-Cyclotetrahydropyrimidinone Nucleoside

Rao, Kambhampati V. B.,Marquez, Victor E.,Kelley, James A.,Corcoran, Mary T.

, p. 127 - 130 (2007/10/02)

A specific and efficient synthesis for 3-(β-D-ribofuranosyl)uracil, isouridine (1), has been devised.Starting with the easily accessible 1-(β-D-ribofuranosyl)-1,2-dihydropyrimidin-2-one (3b) the C-6 carbonyl function of isouridine was built via formation

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