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182565-27-1

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182565-27-1 Usage

General Description

4-Fluoro-alpha-Methylbenzyl Isothiocyanate is a synthetic, organic compound typically characterized by its fluorobenzyl group and isothiocyanate function. A relatively less-studied chemical, it belongs to the family of isothiocyanates, compounds known for their bioactive properties, particularly in anti-cancer activities. Isothiocyanates commonly exist in cruciferous vegetables like broccoli and Brussels sprouts. While specific data about 4-Fluoro-alpha-Methylbenzyl Isothiocyanate are quite limited, the chemical's attributes suggest potential for biomedical application, though this would need further exploration and verification. Its toxicity and environmental impact are also undetermined.

Check Digit Verification of cas no

The CAS Registry Mumber 182565-27-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,2,5,6 and 5 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 182565-27:
(8*1)+(7*8)+(6*2)+(5*5)+(4*6)+(3*5)+(2*2)+(1*7)=151
151 % 10 = 1
So 182565-27-1 is a valid CAS Registry Number.

182565-27-1 Well-known Company Product Price

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  • Alfa Aesar

  • (L12123)  (±)-1-(4-Fluorophenyl)ethyl isothiocyanate, 97%   

  • 182565-27-1

  • 1g

  • 1208.0CNY

  • Detail

182565-27-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-fluoro-4-(1-isothiocyanatoethyl)benzene

1.2 Other means of identification

Product number -
Other names -

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:182565-27-1 SDS

182565-27-1Relevant articles and documents

Electrochemical Benzylic C(sp3)-H Isothiocyanation

Guo, Weisi,Li, Ming,Li, Yufeng,Wang, Tao,Wen, Lirong,Zhang, Shanxue

supporting information, p. 1742 - 1746 (2022/03/14)

Selective C(sp3)-H isothiocyanation represents a significant strategy for the synthesis of isothiocyanate derivatives. We report herein an electrochemical benzylic isothiocyanation in a highly chemo- and site-selective manner under external oxidant-free conditions. The high chemoselectivity is attributed to the facile in situ isomerization of benzylic thiocyanates to isothiocyanates. Notably, the method exhibits high functional group compatibility and is suitable for late-stage functionalization of bioactive molecules.

Synthesis and antitumor activity of optically active thiourea and their 2-aminobenzothiazole derivatives: A novel class of anticancer agents

Manjula,Malleshappa Noolvi,Vipan Parihar,Manohara Reddy,Ramani, Vijay,Gadad, Andanappa K.,Singh, Gurdial,Gopalan Kutty,Mallikarjuna Rao

experimental part, p. 2923 - 2929 (2009/09/30)

A novel series of optically active 2-aminobenzothiazole derivatives were synthesized by reaction of optically active amine (I) with thiophosgene to obtain optically active isothiocyanates (IIa-h) which on condensation with 4-fluoro-3-chloro aniline (III)

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