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ethyl-9-iodononate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57267-52-4

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57267-52-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57267-52-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,2,6 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 57267-52:
(7*5)+(6*7)+(5*2)+(4*6)+(3*7)+(2*5)+(1*2)=144
144 % 10 = 4
So 57267-52-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H21IO2/c1-2-14-11(13)9-7-5-3-4-6-8-10-12/h2-10H2,1H3

57267-52-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 9-iodononanoate

1.2 Other means of identification

Product number -
Other names Ethyl-9-iodononate

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:57267-52-4 SDS

57267-52-4Downstream Products

57267-52-4Relevant academic research and scientific papers

Syntheses and potato tuber-inducing activities of unnatural long-chain OPC-9:0 and OPC-10:0

Toshima, Hiroaki,Takano, Yuko,Ichihara, Akitami,Koda, Yasunori,Kikuta, Yoshio

, p. 1484 - 1487 (1999)

The unnatural long-chain OPCs, OPC-9:0 and OPC-10:0, were respectively synthesized from the ethyl esters of OPC-7:0 and OPC-8:0. C2-carbon elongation was achieved via alkylation of the enolate of tert-butyl acetate. The potato tuber-inducing activity of OPC-10:0, as well as OPC-8:0, -6:0 and -4:0, was similar to that of jasmonic acid. OPC-9:0 also exhibited weak tuber-inducing activity.

Synthesis of 13-oxo-(Z)-9-octadecenoic acid and 15-oxo-(Z)-11-icosenoic acid, arrestants of Oryzaephilus surinamensis L.

Nakajima,Okamura,Takeda,Sugawa,Tateishi,Iwasa,Baba

, p. 551 - 552 (2007/10/03)

Two arrestants of the sawtoothed grain beetle (Oryzaephilus surinamensis L.), 13-oxo-(Z)-9-octadecenoic acid and 15-oxo-(Z)-11-icosenoic acid, were synthesized for the first time by utilizing a Z-selective Wittig reaction.

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