6967-47-1 Usage
Description
ETHYL 2-CYANOVALERATE is a clear, colorless liquid with a fruity odor, known for its versatility in various industries due to its unique chemical properties. It is recognized for its use as a flavoring agent, fragrance, and as a precursor in the synthesis of a range of products, including pharmaceuticals, agrochemicals, and specialty chemicals.
Uses
Used in the Food Industry:
ETHYL 2-CYANOVALERATE is used as a flavoring agent for its distinctive fruity scent, enhancing the taste and aroma of various food products.
Used in the Personal Care Industry:
ETHYL 2-CYANOVALERATE is used as a fragrance in personal care products, adding a pleasant scent to items such as perfumes, soaps, and lotions.
Used in the Pharmaceutical Industry:
ETHYL 2-CYANOVALERATE is used as a precursor in the synthesis of pharmaceuticals, contributing to the development of new medications and therapeutic agents.
Used in the Agrochemical Industry:
ETHYL 2-CYANOVALERATE is used as a chemical building block in the production of agrochemicals, playing a role in the creation of pesticides and other agricultural products.
Used in the Specialty Chemicals Industry:
ETHYL 2-CYANOVALERATE is used as a precursor in the synthesis of other specialty chemicals, highlighting its importance in the chemical manufacturing process.
It is crucial to handle ETHYL 2-CYANOVALERATE with care and adhere to safety guidelines to ensure the safe and effective use of this chemical in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 6967-47-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,6 and 7 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6967-47:
(6*6)+(5*9)+(4*6)+(3*7)+(2*4)+(1*7)=141
141 % 10 = 1
So 6967-47-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H13NO2/c1-3-5-7(6-9)8(10)11-4-2/h7H,3-5H2,1-2H3
6967-47-1Relevant articles and documents
Synthesis of variously 9,9-dialkylated octahydropyrimido [3,4-a]-s-triazines with potential antifungal activity
Ghaib, Amar,Menager, Sabine,Verite, Philippe,Lafont, Olivier
, p. 109 - 116 (2007/10/03)
9,9-Dialkyloctahydropyrimido[3,4-a]-s-triazines were synthesized by iminodimethylation reaction between a 5,5-dialkyl-6-aminopyrimidine-2,4(3H,5H)-dione, a substituted aniline and two moles of formaldehyde. The synthesis of 5,5-dialkyl-6-aminopyrimidinedione consisted of the condensation of urea with ethyl 2,2-dialkylcyanoacetates. 18 Octahydropyrimido[3,4-a]-s-triazines were synthesized and compounds resulting from a supplementary aminomethylation were also obtained. Most of these compounds were tested for antifungal activity in vitro. Only 9,9-dibutyl-6,8-dioxo-3(2-chlorophenyl)2,3,4,5,6,7,8,9-octahydropyrimido[3, 4-a]-s-triazine showed some activity against Microsporum canis.
Stereospecific and Stereoselective Reactions. V. Alkylation of Active Methylene Compounds by the Use of Alcohols, Diethyl Azodicarboxylate, and Triphenylphosphine
Kurihara, Toshio,Sugizaki, Masaru,Kime, Itaru,Wada, Makoto,Mitsunobu, Oyo
, p. 2107 - 2112 (2007/10/02)
The reagent formed by the reaction of diethyl azodicarboxylate (1) and triphenylphosphine (2) reacted with alcohols and ethyl cyanoacetate (6) to give alkylated products in 30 - 80percent yields.When ethyl acetoacetate, 1,3-1,3-coclopentanedione, or 1,3-cyclohexanedione was used in place of 6, the corresponding O-alkylated products were obtained.The reaction of either (S)-(-)-ethyl lactate or (S)-(-)-ethyl 2-hydroxy-3-phenylpropionate with 1, 2, and 6, followed by hydrolysis resulted in the formation of (S)-(-)-methylsuccinic acid or (S)-(-)-benzylsuccinic acid.The results indicate that nearly complete inversion of the configuration takes place in the alkylation step.