86212-34-2 Usage
Description
meso-1,2-Bis(4-chlorophenyl)ethylenediamine, min. 98% is a high-purity chemical compound consisting of two 4-chlorophenyl groups attached to an ethylenediamine molecule in a meso configuration. Its high purity and specific stereochemistry make it a valuable reagent in various industrial and laboratory applications.
Uses
Used in Pharmaceutical Industry:
meso-1,2-Bis(4-chlorophenyl)ethylenediamine, min. 98% is used as a building block for the synthesis of various pharmaceuticals due to its high purity and specific stereochemistry, enabling the production of high-quality and effective drugs.
Used in Agrochemical Industry:
meso-1,2-Bis(4-chlorophenyl)ethylenediamine, min. 98% is used as a key intermediate in the synthesis of agrochemicals, contributing to the development of effective and safe pesticides and other agricultural products.
Used in Organic Synthesis:
meso-1,2-Bis(4-chlorophenyl)ethylenediamine, min. 98% is used as a versatile reagent in organic synthesis, allowing for the creation of a wide range of organic compounds with minimal impurities and specific stereochemical control.
Used in Fine Chemicals Production:
meso-1,2-Bis(4-chlorophenyl)ethylenediamine, min. 98% is used as a crucial component in the production of fine chemicals, including specialty chemicals and high-value compounds for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 86212-34-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,2,1 and 2 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 86212-34:
(7*8)+(6*6)+(5*2)+(4*1)+(3*2)+(2*3)+(1*4)=122
122 % 10 = 2
So 86212-34-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H14Cl2N2/c15-11-5-1-9(2-6-11)13(17)14(18)10-3-7-12(16)8-4-10/h1-8,13-14H,17-18H2/p+2/t13-,14+
86212-34-2Relevant articles and documents
MDM2 DEGRADERS AND USES THEREOF
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Paragraph 00868; 00871-00872, (2021/09/26)
The present invention relates to compounds and methods useful for the modulation of mouse double minute 2 homolog ("MDM2") protein via ubiquitination and/or degradation by compounds according to the present invention.
Dimer ester micromolecule PROTACs for inducing MDM2 to self-degrade E3 ubiquitin ligase
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Paragraph 0133; 0148; 0149; 0168, (2018/10/19)
The invention provides dimer ester micromolecule PROTACs for inducing MDM2 to self-degrade E3 ubiquitin ligase. The structure of the PROTACs is shown in the specification, wherein in a compound (I), L1 is C1-C30 linear or branched alkyl with or without a substituent group, and any carbon atom in L1 is optionally replaced by heteroatom; R1, R2, R3 and R4 are C1-C30 linear or branched alkyl with orwithout a substituent group, C1-C30 aryl with or a without substituent group, C1-C30 linear or branched alkylaryl with or without a substituent group or C1-C30 linear or branched aryl alkyl with or without a substituent group respectively and independently; X1, X2, X3 and X4 are halogen respectively and independently.
Small Molecules Simultaneously Inhibiting p53-Murine Double Minute 2 (MDM2) Interaction and Histone Deacetylases (HDACs): Discovery of Novel Multitargeting Antitumor Agents
He, Shipeng,Dong, Guoqiang,Wu, Shanchao,Fang, Kun,Miao, Zhenyuan,Wang, Wei,Sheng, Chunquan
, p. 7245 - 7260 (2018/08/03)
p53-Murine double minute 2 (MDM2) interaction and histone deacetylases (HDACs) are important targets in antitumor drug development. Inspired by the synergistic effects between MDM2 and HDACs, the first MDM2/HDACs dual inhibitors were identified, which sho
