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5471-50-1

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5471-50-1 Usage

General Description

3,7-dimethyloct-6-enyl 2-chloroacetate is an organic compound with the chemical formula C12H21ClO2. It is a chloroacetate ester with a branched alkyl chain and a double bond in the carbon backbone. 3,7-dimethyloct-6-enyl 2-chloroacetate is used as a chemical intermediate in the synthesis of various organic and pharmaceutical compounds. It is also used in the production of flavor and fragrance compounds. 3,7-dimethyloct-6-enyl 2-chloroacetate is a colorless to pale yellow liquid with a characteristic odor and is typically stored and handled under controlled conditions to prevent degradation or potential hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 5471-50-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,7 and 1 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5471-50:
(6*5)+(5*4)+(4*7)+(3*1)+(2*5)+(1*0)=91
91 % 10 = 1
So 5471-50-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H21ClO2/c1-10(2)5-4-6-11(3)7-8-15-12(14)9-13/h5,11H,4,6-9H2,1-3H3

5471-50-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,7-dimethyloct-6-enyl 2-chloroacetate

1.2 Other means of identification

Product number -
Other names 3,7-dimethyloct-6-en-1-yl chloroacetate

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:5471-50-1 SDS

5471-50-1Downstream Products

5471-50-1Relevant articles and documents

Novel N-4-Piperazinyl Ciprofloxacin-Ester Hybrids: Synthesis, Biological Evaluation, and Molecular Docking Studies

Mahdavi, M.,Mostafavi, H.,Shahbazi, A.,Zarrini, G.

, p. 1558 - 1565 (2020/09/21)

Abstract: A series of novel N-4-piperazinylciprofloxacin-ester hybrids has been synthesized and the structures confirmed by1H and 13C NMR, FT-IRspectral data, and elemental analysis. The products have been tested in vitro for their antibacterial activity againstsix bacterial strains (MRSA, Staphylococcusepidermidis, Bacillussubtilis, Escherichia coli,Salmonella enterica, and Klebsiella pneumoniae) and have demonstrated goodantibacterial activity with MIC values range 6.25–200 μg/mL. Antifungal andcytotoxic activities of the products have been tested against Candida kefyr and human leukemia K562 cell line,respectively. All compounds inhibit growth of K562 cells more efficiently thanthe parent ciprofoxacin in a dose- and duration-dependent way. Molecular dockingstudies performed for the compound 3i indicatesthat similarly to ciprofloxacin it can act as an inhibitor of S. aureus DNA gyrase.

Fragrance alcohol-releasing polysiloxane

-

Page/Page column 10, (2008/06/13)

Organopolysiloxanes which contain a fragrance alcohol Y—OH bonded via a betaine ester group having the structure —N+R1R2—CH2—C(O)OY, cleave off the fragrance alcohol under acid conditions and are resistant to hydrolysis in the neutral and weakly basic range. The organopolysiloxanes adhere to textile fibres, skin or hair and are suitable as perfume components for textile treatment agents and personal care products.

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