Cas 29417-80-9,Methyl-2-methyl-3-p-fluorphenylpropionat

29417-80-9

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Basic information

Product Name: Methyl-2-methyl-3-p-fluorphenylpropionat
Synonyms: Methyl-2-methyl-3-p-fluorphenylpropionat
CAS NO:29417-80-9
Molecular Formula:
Molecular Weight: 196.221
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Methyl-2-methyl-3-p-fluorphenylpropionat(CAS DataBase Reference)
NIST Chemistry Reference: Methyl-2-methyl-3-p-fluorphenylpropionat(29417-80-9)
EPA Substance Registry System: Methyl-2-methyl-3-p-fluorphenylpropionat(29417-80-9)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 29417-80-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 29417-80-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,4,1 and 7 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 29417-80:
(7*2)+(6*9)+(5*4)+(4*1)+(3*7)+(2*8)+(1*0)=129
129 % 10 = 9
So 29417-80-9 is a valid CAS Registry Number.

29417-80-9Upstream product

29417-80-9Downstream Products

29417-80-9Relevant academic research and scientific papers

C?Boron Enolates Enable Palladium Catalyzed Carboboration of Internal 1,3-Enynes

Chrostowska, Anna,Lamine, Walid,Li, Bo,Liu, Shih-Yuan,Miqueu, Karinne,Sotiropoulos, Jean-Marc,Wang, Ziyong,Wu, Jason

supporting information, p. 21231 - 21236 (2021/09/02)

A new family of carbon-bound boron enolates, generated by a kinetically controlled halogen exchange between chlorocatecholborane and silylketene acetals, is described. These C?boron enolates are demonstrated to activate 1,3-enyne substrates in the presence of a Pd0/Senphos ligand complex, resulting in the first examples of a carboboration reaction of an alkyne with enolate-equivalent nucleophiles. Highly substituted dienyl boron building blocks are produced in excellent site-, regio-, and diastereoselectivity by the described catalytic cis-carboboration reaction.

Preparation method for indanone compound

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Paragraph 0097-0099, (2018/08/28)

The invention especially relates to a preparation method for an indanone compound, belonging to the field of organic synthesis. The preparation method for the indanone compounds comprises the following steps: 1) subjecting a compound as shown in a formula I and a compound as shown in a formula II to a condensation reaction so as to prepare a compound as shown in a formula III; 2) subjecting the compound as shown in the formula III to hydrolysis in the presence of alkali so as to prepare a compound as shown in a formula IV; and 3) carrying out acylation and ring closure on the compound as shownin the formula IV so as to prepare the as shown in a formula V. Compared with the prior art, the preparation method for the indanone compound in the invention has the advantages of low raw material cost, simple operation, low production of waste water, waste gas and industrial residues, high yield and the like, and is more suitable for industrial production; and compared with various traditionalpreparation methods for the indanone compound, the preparation method of the invention has obvious advantages and shows good industrialization prospects.

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