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isobornyl acrylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

136374-53-3

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136374-53-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 136374-53-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,3,7 and 4 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 136374-53:
(8*1)+(7*3)+(6*6)+(5*3)+(4*7)+(3*4)+(2*5)+(1*3)=133
133 % 10 = 3
So 136374-53-3 is a valid CAS Registry Number.

136374-53-3Downstream Products

136374-53-3Relevant academic research and scientific papers

Ruthenium(II) Catalysed Highly Regioselective C-3 Alkenylation of Indolizines and Pyrrolo[1,2-a]quinolines

Jadhav, Pankaj Pandit,Kahar, Nilesh Machhindra,Dawande, Sudam Ganpat

, p. 7831 - 7835 (2019)

Discovered the Ruthenium(II) catalysed highly stereo- and regioselective protocol for the oxidative C-3 alkenylation of indolizines and pyrrolo[1,2-a]quinolines. The methodology represents the first example for the directing group assisted C–C bond formation reaction of the indolizines. Under mild reaction conditions, this method provides an ample substrate scope to produce C-3 alkenyl indolizines in excellent to moderate yields. However, pyrrolo[1,2-a]quinolines underwent alkenynation at elevated temperature to furnish C-3 alkenyl derivatives. The functionalized indolizines were selectively reduced to obtain their saturated derivatives.

Preparation method of bio-derived isobornyl (meth) acrylate

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Paragraph 0033-0036; 0041-0044; 0049-0052, (2021/01/15)

The invention belongs to the technical field of photocatalytic organic synthesis, and discloses a preparation method of bio-derived isobornyl (meth) acrylate. The method comprises the following steps:adding camphene, (methyl) acrylic acid, a polymerization inhibitor and a catalyst into a transparent reactor, uniformly mixing, placing under UV light irradiation, carrying out a stirring reaction, and carrying out reduced pressure rotary evaporation after the reaction is finished to obtain isobornyl acrylate and isobornyl methacrylate. According to the method, isobornyl (meth) acrylate is prepared by adopting a photocatalysis method, wherein the reaction conditions are mild, the reaction time is short, side reactions and byproducts are avoided, the conditions of high temperature, high pressure and the like are not needed, the separation and purification are simple and easy to operate, and the isobornyl (meth) acrylate can be obtained. According to the invention, isobornyl (meth) acrylateis prepared from a natural renewable resource camphene, so that a new application direction is opened up for the natural renewable resource vegetable oil, the economic value of the vegetable oil is improved, and the method has a good popularization effect on the development of agriculture and forestry economy.

BLOCK POLYMER, COSMETIC COMPOSITION COMPRISING IT AND COSMETIC TREATMENT PROCESS

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, (2010/02/17)

A block polymer containing, in a block with a Tg greater than 20° C., at least one monomer of formula (I): The invention also relates to a cosmetic composition comprising the block polymer in a cosmetically acceptable medium, and also to a cosmetic process for treating keratin materials using the composition, and most particularly to a process for making up the lips.

BLOCK POLYMER, COSMETIC COMPOSITION COMPRISING IT AND COSMETIC TREATMENT PROCESS

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, (2010/08/03)

A block polymer containing, in a block with a Tg of less than 20° C., at least one monomer of formula (I): The invention also relates to a cosmetic composition containing the block polymer in a cosmetically acceptable medium, and also to a cosmetic process for treating keratin materials using the composition, and most particularly to a process for making up the lips.

Method of manufacturing isobornyl (meth)acrylate

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, (2008/06/13)

The subject invention pertains to a method of manufacturing isobornyl acrylate or isobornyl methacrylate by reacting camphene with acrylic acid or methacrylic acid, respectively, in the presence of a molybdenum heteropolyacid as a catalyst.

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