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(Z)-4-Dodecenoic acid, also known as (Z)-4-Dodec-4-enoic acid, is a naturally occurring unsaturated fatty acid with the chemical formula C12H22O2. It is a positional isomer of dodecenoic acid, featuring a double bond between the 4th and 5th carbon atoms in a 12-carbon chain. (Z)-4-Dodecenoic acid is an important intermediate in the synthesis of various chemicals and pharmaceuticals, and it is also found in some natural products, such as plant oils and waxes. (Z)-4-Dodecenoic acid is characterized by its distinct chemical properties, including its ability to undergo addition reactions due to the presence of the double bond, and it plays a role in various biological processes and industrial applications.

7089-43-2

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7089-43-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7089-43-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,8 and 9 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7089-43:
(6*7)+(5*0)+(4*8)+(3*9)+(2*4)+(1*3)=112
112 % 10 = 2
So 7089-43-2 is a valid CAS Registry Number.

7089-43-2SDS

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 dodec-4c-enoic acid

1.2 Other means of identification

Product number -
Other names Lindersaeure

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:7089-43-2 SDS

7089-43-2Relevant academic research and scientific papers

NEW SYNTHETIC METHOD OF (Z)-4-ALKENOIC ACIDS USING RING-OPENING REACTION OF (Z)-4-HEXENOLIDE WITH ORGANOCOPPER REAGENT

Fujisawa, Tamotsu,Umezu, Kazuto,Kawashima, Masatoshi

, p. 1795 - 1798 (2007/10/02)

(Z)-4-Hexenolide reacted regioselectively with diorganocuprates to give (Z)-4-alkenoic acids in high yields.Synthetic utility was demonstrated by the convenient synthesis of cis-jasmone.

ONE-POT SYNTHESIS OF (Z)-4-ALKENOIC ACIDS

Fujisawa, Tamotsu,Sato, Toshio,Kawara, Tatsuo,Naruse, Kouichi

, p. 1123 - 1124 (2007/10/02)

The reaction of β-propiolactone with di-(Z)-1-alkenylcuprates, prepared from Grignard reagents, copper(I) iodide and acetylene, gave (Z)-4-alkenoic acids in high yields in one-pot operation.

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