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66270-36-8 Usage

General Description

The solvolysis rate constants of 2,2,2-trichloro-1,1-dimethylethyl chloroformate in binary and pure solvents was studied.

Check Digit Verification of cas no

The CAS Registry Mumber 66270-36-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,2,7 and 0 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 66270-36:
(7*6)+(6*6)+(5*2)+(4*7)+(3*0)+(2*3)+(1*6)=128
128 % 10 = 8
So 66270-36-8 is a valid CAS Registry Number.
InChI:InChI=1/C5H6Cl4O2/c1-4(2,5(7,8)9)11-3(6)10/h1-2H3

66270-36-8 Well-known Company Product Price

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  • Aldrich

  • (226505)  2,2,2-Trichloro-1,1-dimethylethylchloroformate  96%

  • 66270-36-8

  • 226505-5G

  • 872.82CNY

  • Detail
  • Aldrich

  • (226505)  2,2,2-Trichloro-1,1-dimethylethylchloroformate  96%

  • 66270-36-8

  • 226505-25G

  • 3,127.41CNY

  • Detail

66270-36-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (1,1,1-trichloro-2-methylpropan-2-yl) carbonochloridate

1.2 Other means of identification

Product number -
Other names 2,2':5',2''-TERTHIOPHENE-5-BORONIC ACID PINACOL 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:66270-36-8 SDS

66270-36-8Downstream Products

66270-36-8Relevant articles and documents

Versatile Cp*Co(III)(LX) Catalyst System for Selective Intramolecular C-H Amidation Reactions

Chang, Sukbok,Jung, Hoimin,Kim, Dongwook,Lee, Jeonghyo,Lee, Jia,Park, Juhyeon

supporting information, p. 12324 - 12332 (2020/08/06)

Herein, we report the development of a tailored cobalt catalyst system of Cp*Co(III)(LX) toward intramolecular C-H nitrene insertion of azidoformates to afford cyclic carbamates. The cobalt complexes were easy to prepare and bench-stable, thus offering a convenient reaction protocol. The catalytic reactivity was significantly improved by the electronic tuning of the bidentate LX ligands, and the observed regioselectivity was rationalized by the conformational analysis and DFT calculations of the transition states. The superior performance of the newly developed cobalt catalyst system could be broadly applied to both C(sp2)-H and C(sp3)-H carbamation reactions under mild conditions.

A NEW PROTECTING TACTICS FOR THE URACIL RESIDUE IN OLIGORIBONUCLEOTIDE SYNTHESIS

Kamimura, Takashi,Masegi, Tsukio,Urakami, Ken-ichi,Honda, Shinkichi,Sekine, Mitsuo,Hata, Tsujiaki

, p. 1051 - 1054 (2007/10/02)

Four kinds of acyl groups as protecting group for the uracil imide function have been examined.Among them, the anisoyl group was found to be most promissing and used to demonstrate the synthesis of the dimer, UpUp.

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