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4335-26-6

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4335-26-6 Usage

General Description

2-(2-Iminothiazolidin-3-yl)-1-phenylethan-1-one monohydrobromide is a chemical compound that is derived from thiazolidine and has a molecular formula of C11H12BrNOS. It is a monohydrobromide salt form of a compound with potential antineoplastic and immunomodulating activities. 2-(2-Iminothiazolidin-3-yl)-1-phenylethan-1-one monohydrobromide may cause growth inhibition and apoptosis in various cancer cell lines, including human non-small cell lung cancer cells, and may inhibit the proliferation of vascular endothelial cells. Additionally, it may inhibit the production of prostaglandin E2 and tumor necrosis factor-alpha in macrophages, as well as increase the production of interleukin-4 in T helper 2 (Th2) cells, leading to a shift in the cytokine balance from T helper 1 (Th1) towards Th2 immune response.

Check Digit Verification of cas no

The CAS Registry Mumber 4335-26-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,3 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4335-26:
(6*4)+(5*3)+(4*3)+(3*5)+(2*2)+(1*6)=76
76 % 10 = 6
So 4335-26-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H12N2OS.BrH/c12-11-13(6-7-15-11)8-10(14)9-4-2-1-3-5-9;/h1-5,12H,6-8H2;1H/b12-11-;

4335-26-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-imino-1,3-thiazolidin-3-yl)-1-phenylethanone,hydrobromide

1.2 Other means of identification

Product number -
Other names EINECS 224-377-8

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:4335-26-6 SDS

4335-26-6Relevant articles and documents

DIHYDRO-5,6 IMIDAZOTHIAZOLES, DIHYDRO-2,3 IMIDAZOBENZOTHIAZOLES, ANALOGUES DU LEVAMISOLE

Amarouch, H.,Loiseau, P. R.,Bonnafous, M.,Caujolle, R.,Payard, M.,et al.

, p. 421 - 438 (2007/10/02)

New compounds containing 5,6-dihydro imidazothiazole 2,3,5,6-tetrahydro imidazothiazole and 2,3-dihydro imidazobenzothiazole rings, substituted by heterocycles analogue to chromones, were synthesized and screened against three nematodes, in vitro.The results indicate moderate anthelmintic properties, compared to levamisole; nevertheless, some products exhibit a significant degree of activity.

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