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55644-06-9

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55644-06-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55644-06-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,6,4 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 55644-06:
(7*5)+(6*5)+(5*6)+(4*4)+(3*4)+(2*0)+(1*6)=129
129 % 10 = 9
So 55644-06-9 is a valid CAS Registry Number.

55644-06-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name benzoic acid,1,4-dioxan-2-ol

1.2 Other means of identification

Product number -
Other names 1,4-dioxan-2-ylbenzoate

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:55644-06-9 SDS

55644-06-9Relevant articles and documents

Transformation of Metal-Organic Frameworks into Stable Organic Frameworks with Inherited Skeletons and Catalytic Properties

Chen, Kai,Wu, Chuan-De

, p. 8119 - 8123 (2019)

Metal-organic frameworks (MOFs) are an emerging class of porous materials with attractive properties, however, their practical applications are heavily hindered by their fragile nature. We report herein an effective strategy to transform fragile coordinat

Microwave-Enhanced Coupling of Carboxylic Acids with Liquid Ketones and Cyclic Ethers Using Tetrabutylammonium Iodide/ t-Butyl Hydroperoxide

Macías-Benítez, Pablo,Moreno-Dorado, F. Javier,Guerra, Francisco M.

, p. 6027 - 6043 (2020/05/22)

The oxidative coupling of carboxylic acids with liquid ketones and cyclic ethers has been accomplished in minutes using t-butyl hydroperoxide in the presence of tetrabutylammonium iodide under microwave irradiation in the absence of a solvent. In addition to drastically shortening the reaction times, the use of microwaves resulted, in general, in yields equal to or higher than those obtained by conventional heating.

Iron porphyrin-catalyzed C(SP3) -H activation for the formation of C–O bond via cross-dehydrogenative coupling of cycloether and aromatic acid

Wen, Wei-Hong,Xie, An-Na,Wang, Hua-Hua,Zhang, Dong-Xu,Ali, Atif,Ying, Xiao,Liu, Hai-Yang

, p. 7169 - 7176 (2017/11/17)

An efficient cyclic ether benzoxylation was achieved by using iron porphyrin as the catalyst and di-tert-butyl peroxide oxidant. The benzoic acid substrates bearing electron donating or withdrawing groups could react with cyclic ether smoothly to afford t

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