Welcome to LookChem.com Sign In|Join Free

CAS

  • or

15666-97-4

Post Buying Request

15666-97-4 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

15666-97-4 Usage

Chemical Properties

Colorless liquid

Uses

Octyl cyanoacetate may be used in the preparation of a small molecule with a dithienosilole core for the high efficiency solution-processed organic photovoltaic cells. It may be used in the preparation of small molecule DCAO3TBDT with the acceptor-donor-acceptor (A-D-A) structure and benzo[1,2-b:4,5-b′]dithiophene (BDT) as the central building block.

Check Digit Verification of cas no

The CAS Registry Mumber 15666-97-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,6,6 and 6 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 15666-97:
(7*1)+(6*5)+(5*6)+(4*6)+(3*6)+(2*9)+(1*7)=134
134 % 10 = 4
So 15666-97-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H19NO2/c1-2-3-4-5-6-7-10-14-11(13)8-9-12/h2-8,10H2,1H3

15666-97-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name octyl 2-cyanoacetate

1.2 Other means of identification

Product number -
Other names Octyl cyanoacetate

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:15666-97-4 SDS

15666-97-4Synthetic route

octanol
111-87-5

octanol

cyanoacetic acid
372-09-8

cyanoacetic acid

octyl 2-cyanoacetate
15666-97-4

octyl 2-cyanoacetate

Conditions
ConditionsYield
With magnesium sulfate; zinc(II) perchlorate at 80℃; for 40h;95%
With sulfuric acid In benzene for 3h; Heating;86.8%
With toluene-4-sulfonic acid In benzene Heating;85%
With toluene-4-sulfonic acid In benzene at 120℃; for 24h; Dean-Stark;81.1%
With toluene-4-sulfonic acid In toluene at 80 - 125℃; Reagent/catalyst;
n-octyl triflate
71091-89-9

n-octyl triflate

dicyclohexylammonium α-cyanoacrylate

dicyclohexylammonium α-cyanoacrylate

A

n-octyl 2-cyanoacrylate

n-octyl 2-cyanoacrylate

B

di-n-octyl ether
629-82-3

di-n-octyl ether

C

CHF3O3S*C12H23N
1215021-90-1

CHF3O3S*C12H23N

D

octyl 2-cyanoacetate
15666-97-4

octyl 2-cyanoacetate

E

2-cyanoacrylic acid
15802-18-3

2-cyanoacrylic acid

Conditions
ConditionsYield
With trifluoroacetic acid In dichloromethane at 22℃; Product distribution / selectivity;A 65%
B n/a
C n/a
D n/a
E n/a
octyl (3S)-(+)-3-hydroxypentanoate
92445-22-2

octyl (3S)-(+)-3-hydroxypentanoate

octyl 2-cyanoacetate
15666-97-4

octyl 2-cyanoacetate

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 97.2 percent / p-TsOH / CH2Cl2 / 1 h / Ambient temperature
2: LiAlH4 / diethyl ether / 4 h / Ambient temperature
3: 86.8 percent / c.c.H2SO4 / benzene / 3 h / Heating
View Scheme

15666-97-4Related news

A star-shaped oligothiophene with triphenylamine as core and Octyl cyanoacetate (cas 15666-97-4) as end groups for solution-processed organic solar cells09/01/2019

A new star-shaped D–π–A molecule with triphenylamine (TPA) as core and donor unit, octyl cyanoacetate (CA) as end group and acceptor unit, and 2,2′-bithiophene vinylene (bTV) as π bridge, S(TPA-bTV-CA) was designed and synthesized for the application as donor materials in solution-processed...detailed

15666-97-4Relevant articles and documents

Method for preparing glue and medical glue

-

Paragraph 0082-0085, (2018/06/26)

The present invention provides a method for preparing an acrylate based adhesive in high purity, which performs a process of producing an alkyl cyanoacrylate polymer from alkyl cyanoacetate and a process of depolymerizing the alkyl cyanoacrylate polymer into monomers together to reduce the production costs.(AA) Mix alkyl alcohol with an organic solvent(BB) Add cyanoacetic acid and strong acid to the mixed solution and heating the same for esterification(CC) Remove water produced during the esterification reaction by azeotropic distillation and purify/dry the mixture(DD) Stir alkyl cyanoacetate, a crosslinking agent, and a catalyst to prepare a polymer(EE) Prepare a crude polymer from the polymer(FF) Perform catalytic depolymerization of the crude polymer to obtain a monomer-type high purity polymerCOPYRIGHT KIPO 2018

ALPHA-CYANOACRYLATE ESTER SYNTHESIS

-

Page/Page column 10-12, (2012/04/17)

The high temperatures required for cracking the cyanoacrylate oligomers, produced by the Knovenagel condensation of formaldehyde and a cyanoacetate, limit the synthetic diversity and the number of different side chains that can be incorporated into a cyanoacrylate prepared using this method. Accordingly, the diversity of cyanoacrylate monomers prepared industrially is quite limited. Disclosed herein is a method for the preparation of alpha-Cyanoacrylate ester monomers from a variety of phosphonium and ammonium alpha-cyanoacrylate salts. The phosphonium and ammonium alpha-cyanoacrylate salts are of the general formula: (I).

Structure-activity relationship of new organic NLO materials based on push-pull azodyes. 1: Synthesis and molecular properties of the dyes

Tirelli,Altomare,Solaro,Ciardelli,Meier,Bosshard,Guenter

, p. 122 - 128 (2007/10/03)

Several new push-pull azobenzene dyes were synthesized by diazonium salt coupling of electron-poor anilines with N,N-dialkylanilines. Their dipole moments and first-order hyperpolarizabilities were evaluated respectively from the concentration dependence of the dielectric constant of solutions in apolar solvents and by the electric-field-induced-second-harmonic-generation (EFISH) technique. Investigation of the influence of both nature and steric hindrance of the electron-withdrawing group allowed to highlight a significant deviation from linearity in the relationship between dipole moments and first-order hyperpolarizabilities. This effect was particularly noticeable when multiple electron withdrawing groups pointing in different directions were present on the same phenyl ring. Johann Ambrosius Barth 1998.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 15666-97-4