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70142-79-9

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70142-79-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70142-79-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,1,4 and 2 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 70142-79:
(7*7)+(6*0)+(5*1)+(4*4)+(3*2)+(2*7)+(1*9)=99
99 % 10 = 9
So 70142-79-9 is a valid CAS Registry Number.

70142-79-9SDS

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 4-[[4-[(4-carboxyphenyl)carbamoyl]benzoyl]amino]benzoic acid

1.2 Other means of identification

Product number -
Other names N.N'-Terephthaloyl-bis-<p-amino-benzoesaeure>

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:70142-79-9 SDS

70142-79-9Relevant articles and documents

Syntheses, Structures and Sorption Properties of Three Isoreticular Trinuclear Indium-Based Amide-Functionalized Metal–Organic Frameworks

Zhang, Zong-Hui,Wang, Qian,Xue, Dong-Xu,Bai, Junfeng

, p. 3603 - 3610 (2019)

Amide-functionalized metal–organic frameworks (AFMOFs) as a subclass of MOF materials have received great interest recently because of their intriguing structures and diverse potential applications. In this work, solvothermal reactions between indium nitrate and two mixed-linkers afforded two new isoreticular 8-connected trinuclear indium-based AFMOFs of [(In3O)(OH)(L2)2(IN)2]?(solv)x (2-In) and [(In3O)(OH)(L2)2(AIN)2]?(solv)x (NH2-2-In) (H2L2=4,4′-(carbonylimino)dibenzoic acid and HIN=isonicotinic acid or HAIN=3-aminoisonicotinic acid), respectively. Moreover, by means of reticular chemistry, an extended network of [(In3O)(OH)(L3)2(PB)2]?(solv)x (3-In) (H2L3=4,4′-(terephthaloylbis(azanediyl))dibenzoic acid, HPB=4-(4-pyridyl)benzoic acid) was also successfully realized after prolongation of the former dicarboxylate linker and HIN, resulting in a truly 8-connected isoreticular AFMOF platform. These frameworks were structurally determined by single-crystal X-ray diffraction (SCXRD). Sorption studies further demonstrate that 2-In and NH2-2-In exhibit not only high surface areas and pore volumes but also relatively high carbon capture capabilities (the CO2 uptakes reach 60.0 and 75.5 cm3 g?1 at 298 K and 760 torr, respectively) due to the presences of amide and/or amine functional groups. The selectivity of CO2/N2 and CO2/CH4 calculated by IAST are 10.18 and 12.43, 4.20 and 4.23 for 2-In and NH2-2-In, respectively, which were additionally evaluated by mixed-gases dynamic breakthrough experiments. In addition, high-pressure gas sorption measurements show that both materials could take up moderate amounts of natural gas.

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