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16868-11-4

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16868-11-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16868-11-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,8,6 and 8 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 16868-11:
(7*1)+(6*6)+(5*8)+(4*6)+(3*8)+(2*1)+(1*1)=134
134 % 10 = 4
So 16868-11-4 is a valid CAS Registry Number.
InChI:InChI=1/C13H20O2/c1-5-11(14)15-10-8-9-6-7-13(10,4)12(9,2)3/h5,9-10H,1,6-8H2,2-4H3/t9-,10+,13+/m0/s1

16868-11-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [(1S,3R,4S)-4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl] prop-2-enoate

1.2 Other means of identification

Product number -
Other names Acrylic acid,2-bornyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:16868-11-4 SDS

16868-11-4Relevant articles and documents

Synthesis and biological activity of heterocyclic borneol derivatives

Sokolova, Anastasiya S.,Yarovaya, Оlga I.,Shtro, Anna A.,Borisova, Marina S.,Morozova, Ekaterina A.,Tolstikova, Tatyana G.,Zarubaev, Vladimir V.,Salakhutdinov, Nariman F.

, p. 371 - 377 (2017)

(figure presented) A series of novel heterocyclic derivatives of (–)-borneol has been prepared by the interaction of (1S,2R,4S)-1,7,7-trimethylbicyclo[2.2.1]-heptan-2-yl 2-chloroacetate and (1S,2R,4S)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl 3-chloropropanoate with different N- and S-nucleophiles. The obtained products were screened for antiviral, antiulcer, and analgesic activity.

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.

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