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1131-92-6

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1131-92-6 Usage

Purpose

Antiseptic and disinfectant

Common uses

Pharmaceutical and personal care products (mouthwash, throat sprays, skin cleansers)

Mechanism of action

Disrupts bacterial cell walls, leading to destruction

Effective against

Wide range of bacteria and fungi

Precaution

Can cause skin irritation and allergic reactions in some individuals

Check Digit Verification of cas no

The CAS Registry Mumber 1131-92-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,3 and 1 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1131-92:
(6*1)+(5*1)+(4*3)+(3*1)+(2*9)+(1*2)=46
46 % 10 = 6
So 1131-92-6 is a valid CAS Registry Number.

1131-92-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2,4-Dichloro-benzyl)-guanidine; hydrochloride

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:1131-92-6 SDS

1131-92-6Upstream product

1131-92-6Downstream Products

1131-92-6Relevant articles and documents

INHIBITION OF CELL PROLIFERATION

-

Page/Page column 47; 59; 73, (2008/06/13)

The disclosed modulators of Rb:Raf-1 interactions are potent, selective disruptors of Rb:Raf-1 binding, with IC50 values ranging from 80 nM to 500 nM. Further, these compounds are surprisingly effective in inhibiting a wide variety of cancer cells, including osteosarcoma, epithelial lung carcinoma, non small cell lung carcinoma, three different pancreatic cancer cell lines, two different glioblastoma cell lines, metastatic breast cancer, melanoma, and prostate cancer. Moreover, the disclosed compounds effectively disrupt angiogenesis and significantly inhibited tumors in nude mice derived from human epithelial lung carcinoma tumors. Accordingly, the disclosed compounds, pharmaceutical compositions comprising the compounds, methods of inhibiting cell proliferation, methods of treating subjects with cancer, and methods of preparing the disclosed compounds are provided.

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