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1,2,4,5-Benzenetetracarboxylic acid, 3,6-difluoro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

10311-26-9

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10311-26-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10311-26-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,1 and 1 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10311-26:
(7*1)+(6*0)+(5*3)+(4*1)+(3*1)+(2*2)+(1*6)=39
39 % 10 = 9
So 10311-26-9 is a valid CAS Registry Number.

10311-26-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name difluoropyromellitic acid

1.2 Other means of identification

Product number -
Other names 3,6-Difluorpyromellith-saeure

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:10311-26-9 SDS

10311-26-9Relevant academic research and scientific papers

Benzdiynes (1,2,4,5-tetradehydrobenzenes): Direct observation by wavelength-selective photolyses of benzenetetracarboxylic dianhydrides in low-temperature nitrogen matrixes

Sato, Tadatake,Arulmozhiraja, Sundaram,Niino, Hiroyuki,Sasaki, Shigekuni,Matsuura, Tohru,Yabe, Akira

, p. 4512 - 4521 (2007/10/03)

Toward direct observation of benzdiynes, we investigated the wavelength-selective photolyses of five kinds of benzenetetracarboxylic dianhydride derivatives in nitrogen matrixes at 13 K. In the first step of the photolyses, all dianhydrides were converted into benzynedicarboxylic anhydrides with loss of CO and CO2 upon irradiation at 308 nm. In the second step, the benzyne intermediates were photolyzed at 266 nm. In these photolyses, the generation of two kinds of benzdiynes, 3,6-difluoro-1,4-benzdiyne and 3,6-bis(trifluoromethyl)-1,4-benzdiyne, was confirmed by good correspondence between observed and calculated IR spectra. These benzdiynes were converted into the corresponding hexatriynes upon further irradiation at 266 nm. Benzdiynes were not observed in the photolyses of the other three dianhydrides: only hexatriynes were observed as major photoproducts. These results suggested that benzdiynes were generated first and then converted into hexatriynes and that the efficiency of the decomposition of benzdiynes depended on the substituents. The dynamics of the generation and decomposition of benzdiynes in the matrixes was analyzed by using a successive reaction scheme.

Reactions of tetrafluorophthalic and difluoropyromellitic acids with sulphur tetrafluoride

Dmowski, Wojciech

, p. 251 - 255 (2007/10/02)

Fluorination of tetrafluorophthalic acid (1) with an SF4/HF mixture at 190-300 deg C afforded, beside the expected perfluoro-o-xylene (2) and perfluoro-o-toluyl fluoride (4), considerable amounts of octafluoro-1,3-dihydroisobenzofuran (3).The reaction wit

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