Welcome to LookChem.com Sign In|Join Free

CAS

  • or

13053-89-9

Post Buying Request

13053-89-9 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

13053-89-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13053-89-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,5 and 3 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 13053-89:
(7*1)+(6*3)+(5*0)+(4*5)+(3*3)+(2*8)+(1*9)=79
79 % 10 = 9
So 13053-89-9 is a valid CAS Registry Number.

13053-89-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(pyrimidin-2'-yl)benzamide

1.2 Other means of identification

Product number -
Other names N-(pyrimidin-2-yl)benzamide

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:13053-89-9 SDS

13053-89-9Relevant articles and documents

Blue Fluorescence from BF2 Complexes of N,O-Benzamide Ligands: Synthesis, Structure, and Photophysical Properties

Yamaji, Minoru,Kato, Shin-Ichiro,Tomonari, Kazuhiro,Mamiya, Michitaka,Goto, Kenta,Okamoto, Hideki,Nakamura, Yosuke,Tani, Fumito

, p. 12514 - 12519 (2017)

Small molecules having intense luminescence properties are required to promote biological and organic material applications. We prepared five types of benzamides having pyridine, pyridazine, pyrazine, and pyrimidine rings and successfully converted them i

Copper-Catalyzed Tandem Reactions of 2-Amine-[1,3,5]triazines with Nitriles

Zhang, Li-Yu,Zhang, Chen,Wang, Tao,Shi, Yu-Long,Ban, Meng-Tao,Cui, Dong-Mei

, p. 536 - 543 (2019/01/24)

Copper-catalyzed intermolecular annulation of 2-amine-[1,3,5]triazines and aryl nitriles for the synthesis of [1,2,4]triazolo[1,5-a][1,3,5]triazines via N-C bond formation and oxidative N-N coupling [oxidative 3 + 2 cyclization] is presented. A wide range of aryl nitriles, including electron-rich benzonitriles, electron-poor benzonitriles, 2-cyanothiophene, and 4-cyanopyridine, were all functionalized with 2-amine-[1,3,5]triazines. Furthermore, amidation of 2-amine-[1,3,5]triazines via Cu-catalyzed C-CN bond cleavage of phenylacetonitriles is also demonstrated. The reaction occurred in moderate to satisfactory yields and tolerated alkyl- or aryl-substituted 2-amine-[1,3,5]triazines. Aniline, aminopyridine, and aminopyrimidine also afforded the desired products.

Synthesis method of N-heterocyclic acylamide derivative

-

Paragraph 0066; 0067; 0068, (2019/01/14)

The invention discloses a synthesis method of an N-heterocyclic acylamide derivative. A reaction general formula is as shown in the specification. According to the synthesis method, an imidazo heterocyclic amine compound I is taken as a raw material; unde

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 13053-89-9