1775-43-5 Usage
Description
CIS-3-HEXENOIC ACID, also known as (3Z)-3-Hexenoic Acid, is an unsaturated aliphatic acid characterized by its cis configuration. It is a 3-hexenoic acid with a double bond between the third and fourth carbon atoms, which gives it unique chemical properties and applications in various fields.
Uses
Used in Flavor Chemistry:
CIS-3-HEXENOIC ACID is used as a flavoring agent in the chemistry of flavors. Its unique chemical structure contributes to the development of distinct and complex flavor profiles, making it a valuable component in the creation of various food and beverage products.
Used in Fragrance Industry:
In the fragrance industry, CIS-3-HEXENOIC ACID is utilized as a key ingredient in the formulation of perfumes, colognes, and other scented products. Its ability to create unique and appealing aromas makes it an essential component in the development of new fragrances.
Used in Pharmaceutical Industry:
CIS-3-HEXENOIC ACID also finds applications in the pharmaceutical industry, where it is used as an intermediate in the synthesis of various drugs and pharmaceutical compounds. Its unique chemical properties make it a valuable building block in the development of new medications and therapies.
Used in Cosmetic Industry:
In the cosmetic industry, CIS-3-HEXENOIC ACID is employed as an active ingredient in various skincare and beauty products. Its unique properties contribute to the development of innovative formulations that address specific skin concerns and enhance the overall appearance and health of the skin.
Check Digit Verification of cas no
The CAS Registry Mumber 1775-43-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,7 and 5 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1775-43:
(6*1)+(5*7)+(4*7)+(3*5)+(2*4)+(1*3)=95
95 % 10 = 5
So 1775-43-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H10O2/c1-2-3-4-5-6(7)8/h4-5H,2-3H2,1H3,(H,7,8)/b5-4-
1775-43-5Relevant articles and documents
Directed, regiocontrolled hydroamination of unactivated alkenes via protodepalladation
Gurak, John A.,Yang, Kin S.,Liu, Zhen,Engle, Keary M.
, p. 5805 - 5808 (2016)
A directed, regiocontrolled hydroamination of unactivated terminal and internal alkenes is reported. The reaction is catalyzed by palladium(II) acetate and is compatible with a variety of nitrogen nucleophiles. A removable bidentate directing group is used to control the regiochemistry, prevent β-hydride elimination, and stabilize the nucleopalladated intermediate, facilitating a protodepalladation event. This method affords highly functionalized amino acids in good yields with high regioselectivity.
Enantiodivergent and γ-selective asymmetric allylic amination
Wang, Jianmin,Chen, Jie,Kee, Choon Wee,Tan, Choon-Hong
, p. 2382 - 2386 (2012/05/19)
Double agent: The title reaction using the guanidine catalyst 1 can deliver both enantiomers of the product with excellent enantioselectivity by judicious choice of the double bond geometry of the the β,γ-unsaturated carbonyl compound. Computational studies reveal the possible origin of the inversed enantioselectivity, and the potential for enantiodivergent synthesis chiral amine-containing substrates is attractive. Copyright
Stereoselective catalytic hydrogenation of sorbic acid and sorbic alcohol with new Cp*Ru complexes
Steines, Stephan,Englert, Ulli,Driessen-Hoelscher, Birgit
, p. 217 - 218 (2007/10/03)
The new Cp*Ru complexes [Cp*Ru(η4-MeCH=CHCH=CHCO2H)]+X- (X- = CF3SO3- or [B{C6H3(CF3)2-3,5}4]-) are very effective catalysts for the hydrogenation of sorbic acid to cis-hex-3-enoic acid and of sorbic alcohol to cis-hex-3-en-1-ol (leaf alcohol) under mild conditions in liquid two-phase systems.
