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17271-89-5

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17271-89-5 Usage

General Description

1-(azidomethyl)-4-methylbenzene, also known as SALTDATA: FREE, is a compound with the chemical formula C9H9N3. It is a derivative of toluene, with a methyl group and an azido group attached to the benzene ring. The azido group, which consists of three nitrogen atoms, gives the compound its unique properties and makes it useful in various chemical reactions and synthesis processes. While the specific uses of SALTDATA: FREE are varied, it is commonly employed in organic chemistry as a reagent or precursor for the production of other compounds. Its structure and chemical properties make it an important building block for the synthesis of pharmaceuticals, agrochemicals, and other industrial products. Overall, SALTDATA: FREE is a versatile and valuable chemical compound with wide-ranging applications in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 17271-89-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,2,7 and 1 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 17271-89:
(7*1)+(6*7)+(5*2)+(4*7)+(3*1)+(2*8)+(1*9)=115
115 % 10 = 5
So 17271-89-5 is a valid CAS Registry Number.

17271-89-5 Well-known Company Product Price

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  • Aldrich

  • (742570)  1-(Azidomethyl)-4-methylbenzene solution  ~0.5 M in tert-butyl methyl ether, ≥95.0% (HPLC)

  • 17271-89-5

  • 742570-10ML

  • 1,239.03CNY

  • Detail
  • Aldrich

  • (742570)  1-(Azidomethyl)-4-methylbenzene solution  ~0.5 M in tert-butyl methyl ether, ≥95.0% (HPLC)

  • 17271-89-5

  • 742570-50ML

  • 4,586.40CNY

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17271-89-5SDS

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 1-(Azidomethyl)-4-methylbenzene

1.2 Other means of identification

Product number -
Other names 1-azidomethyl-4-methylbenzene

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:17271-89-5 SDS

17271-89-5Relevant articles and documents

Identification of Phenylphthalazinones as a New Class of Leishmania infantum Inhibitors

Sijm, Maarten,de Heuvel, Erik,Matheeussen, An,Caljon, Guy,Maes, Louis,Sterk, Geert-Jan,de Esch, Iwan J. P.,Leurs, Rob

, p. 219 - 227 (2020)

Leishmaniasis is a neglected parasitic disease caused by over 20 different Leishmania species. Current treatments often rely on harsh regimes of pentavalent antimonials such as sodium stibogluconate, while more recent drugs suffer other shortcomings such

An expedient and highly selective conversion of alcohols to azides using a NaN3/BF3·Et2O system

Kumar, H.M. Sampath,Reddy, B.V. Subba,Anjaneyulu,Yadav

, p. 7385 - 7388 (1998)

Alkyl azides were prepared in good yields by treatment of allylic and benzylic alcohols with a molar equivalent of NaN3 in the presence of BF3·Et2O in dioxane.

Application of magnetic dicationic ionic liquid phase transfer catalyst in nuclophilic substitution ractions of benzyl halides in water

Aghajeri, Manouchehr,Kiasat, Ali Reza,Goodajdar, Bijan Mombeni

, p. 1691 - 1695 (2016)

Magnetic dicationic ionic liquid (MDIL) was successfully prepared and evaluated as phase-transfer catalyst for nucleophilic substitution reactions. The reactions was occurred in water and furnished the corresponding benzyl derivatives in high yields. No evidence for the formation of by-product for example benzyl alcohol of the reaction was observed and the products were obtained in pure form without further purification.

Synthesis and Evaluation of Bakuchiol Derivatives as Potent Anti-inflammatory Agents in Vitro and in Vivo

Bai, Chunmei,Bian, Ming,Du, Huan-Huan,Gong, Guohua,Liu, Chunyan,Ma, Qianqian,Quan, Zhe-Shan,Wei, Chengxi

supporting information, p. 15 - 24 (2022/01/27)

Bakuchiol, a prenylated phenolic monoterpene derived from the fruit of Psoralen corylifolia L. (Buguzhi), is widely used to treat tumors, viruses, inflammation, and bacterial infections. In this study, we designed and synthesized 30 bakuchiol derivatives

Synthesis, Docking, and Biological activities of novel Metacetamol embedded [1,2,3]-triazole derivatives

Battu, Satyanarayana,Joolakanti, Hima Bindhu,Kamepalli, Ramanjaneyulu,Miryala, Jeevanreddy

, (2021/06/18)

ERα controls the breast tissue development and progression of breast cancer. In our search for novel compounds to target Estrogen Receptor Alpha Ligand-Binding Domain, we identified “N-(3-((1H-1,2,3-triazol-4-yl)methoxy)phenyl)acetamide” derivatives as lead compounds. The Docking studies indicated good docking score for Metacetamol derivatives when docked into the 1XP6. A series of metacetamol derivatives have been synthesized, characterized and evaluated for cytotoxicity, anti bacterial and anti oxidant activities. Among the tested twelve hybrid compounds, “7a, 7g, 7h and 7i” derivatives showed promising cytotoxicity with IC50 value of 50 value of 30 μM, whereas Compounds “7a, 7b, 7c, 7d, 7g, 7j, 7k and 7l” showed moderate anti bacterial activity with the MIC value of 300 μM.

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