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149054-67-1

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149054-67-1 Usage

Derivative of

Pyrazole and oxime

Usage

Organic synthesis and as a reagent in chemical reactions

Antimicrobial properties

Strong

Antifungal properties

Strong

Industries

Pharmaceutical and agricultural

Structure

Valuable building block for new compounds with potential medicinal or agricultural applications

Oxime group

Acts as a chelating agent

Metal ion interaction

Forms stable complexes with various metal ions

Additional applications

Utilized in analytical chemistry and metal extraction processes

Check Digit Verification of cas no

The CAS Registry Mumber 149054-67-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,0,5 and 4 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 149054-67:
(8*1)+(7*4)+(6*9)+(5*0)+(4*5)+(3*4)+(2*6)+(1*7)=141
141 % 10 = 1
So 149054-67-1 is a valid CAS Registry Number.

149054-67-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-dimethyl-5-phenoxypyrazole-4-carbaldehyde oxime

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:149054-67-1 SDS

149054-67-1Relevant articles and documents

Identification of antitumor activity of pyrazole oxime ethers

Park, Hyun-Ja,Lee, Kyung,Park, Su-Jin,Ahn, Bangle,Lee, Jong-Cheol,Cho, HeeYeong,Lee, Kee-In

, p. 3307 - 3312 (2007/10/03)

A series of pyrazole oxime ether derivatives were prepared and examined as cytotoxic agents. In particular, 5-phenoxypyrazole was comparable to doxorubicin, while exhibiting very potent cytotoxicity against XF 498 and HCT15.

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