Welcome to LookChem.com Sign In|Join Free
  • or
acetamide, 2-chloro-N-(4,6-dimethoxy-2-pyrimidinyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

181270-85-9

Post Buying Request

181270-85-9 Suppliers

Recommended suppliers

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

181270-85-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 181270-85-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,1,2,7 and 0 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 181270-85:
(8*1)+(7*8)+(6*1)+(5*2)+(4*7)+(3*0)+(2*8)+(1*5)=129
129 % 10 = 9
So 181270-85-9 is a valid CAS Registry Number.

181270-85-9Downstream Products

181270-85-9Relevant academic research and scientific papers

New 2-benzylsulfanyl-nicotinic acid based 1,3,4-oxadiazoles: Their synthesis and biological evaluation

Patel, Navin B.,Purohit, Amit C.,Rajani, Dhanji P.,Moo-Puc, Rosa,Rivera, Gildardo

, p. 677 - 687 (2013/05/09)

A novel series of 5-(2-benzylsulfanyl-pyridin-3-yl)-2-(substituted)- sulfanyl-1,3,4-oxadiazoles 6a-j were synthesized from key intermediate 5-(2-benzylsulfanyl-pyridin-3-yl)-3H-[1,3,4]oxadiazole-2-thione 5. Nucleophilic substitution reactions with differe

Synthesis, biological evaluation and molecular modeling studies of N-aryl-2-arylthioacetamides as non-nucleoside HIV-1 reverse transcriptase inhibitors

Xiaohe, Zhu,Yu, Qin,Hong, Yan,Xiuqing, Song,Rugang, Zhong

experimental part, p. 330 - 339 (2011/12/22)

A series of N-aryl-2-arylthioacetamide derivatives (2-4) designed as non-nucleoside reverse transcriptase inhibitors was synthesized and evaluated for their inhibitory activity against HIV-1 (IIIB) replication in MT-4 cell cultures. The compounds 2-4 were

Synthesis and antitumor activities of novel 1,4-substituted phthalazine derivatives

Zhang, Shu Lan,Liu, Ya Jing,Zhao, Yan Fang,Guo, Qiu Ting,Gong, Ping

scheme or table, p. 1071 - 1074 (2011/10/05)

A series of 1,4-substituted phthalazine derivatives were designed and synthesized. All the prepared compounds were screened for their cytotoxic activities against A549, HT-29 and MDA-MB-231 cell lines in vitro. Among them, compounds 7a-7h showed excellent selectivity for MDA-MB-231 cell line with IC50 values from 1nmol/L to 0.92μmol/L. A preliminary SAR study of these derivatives was performed.

Synthesis and bioactivity of novel triazolo [1,5-a]pyrimidine derivatives[3]

Yang, Guangfu,Xu, Li,Lu, Aihong

, p. 491 - 496 (2007/10/03)

In an attempt to discover novel compounds with high herbicidal activity and low toxicity, a series of novel 1,2,4-triazolo[1,5-a]pyrimidine derivatives, α-(5,7-dimethyl-1,2,4-triazolo[1,5-a]pyrimidine-2-thio)acetamides 3 and α-(5,7-dimethyl-1,2, 4-triazol

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 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 181270-85-9