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Methyl 3-methyl-5-oxohex-2-enoate is a chemical compound with the molecular formula C7H10O3. It is an organic ester derived from the parent compound hex-2-enoic acid, featuring a methyl group at the 3rd carbon and a carbonyl group at the 5th carbon. methyl 3-methyl-5-oxohex-2-enoate is characterized by its conjugated double bond system, which contributes to its reactivity and chemical properties. It is used in the synthesis of various organic compounds and can be found in the fragrance and flavor industry due to its unique scent. The compound is also known for its potential applications in the pharmaceutical sector. Its structure and properties make it a versatile building block in organic chemistry, particularly in the preparation of complex molecules and natural products.

689-17-8

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689-17-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 689-17-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,8 and 9 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 689-17:
(5*6)+(4*8)+(3*9)+(2*1)+(1*7)=98
98 % 10 = 8
So 689-17-8 is a valid CAS Registry Number.

689-17-8Downstream Products

689-17-8Relevant academic research and scientific papers

Two-stage synthesis of 3-(perfluoroalkyl)-substituted vinyldiazocarbonyl compounds and their nonfluorinated counterparts: A comparative study

Supurgibekov, Murat B.,Prakash, G.K. Surya,Nikolaev, Valerij A.

, p. 1215 - 1226 (2013/06/04)

Two approaches for the synthesis of fluorinated (F) and nonfluorinated (H) 4-(alkoxycarbonyl)-substituted cis- and trans-vinyldiazocarbonyl compounds with substituents of variable stereoelectronic nature (H, Me, Ph, CF3, OTBS) at the C-3 atom of the vinyl double bond from the relevant 1,3-dicarbonyl compounds were compared: a pathway using the Wittig reaction followed by a diazo transfer reaction was most efficient for the synthesis of the H-vinyldiazocarbonyl compounds (total yields of up to 60%), while the yields of their F-analogues under similar conditions did not exceed 16-37%. An approach via diazo transfer followed by the Wittig reaction, in contrast, is more effective for the preparation of F-vinyldiazocarbonyl compounds (total yields 37-69%). The configuration of the resulting F- and H-vinyldiazocarbonyl compounds is evidently controlled by the steric bulk of the substituent at the C-3 atom of the vinyl double bond and, in addition, depends on the specific synthetic pathway. Georg Thieme Verlag Stuttgart . New York.

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