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596-31-6

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596-31-6 Usage

Chemical Properties

White Solid

Uses

Different sources of media describe the Uses of 596-31-6 differently. You can refer to the following data:
1. A trityl-cysteine analog as inhibitor of human mitotic kinesin
2. Methyl Triphenylmethyl Ether is a trityl-cysteine analog as inhibitor of human mitotic kinesin.

Synthesis Reference(s)

The Journal of Organic Chemistry, 28, p. 2914, 1963 DOI: 10.1021/jo01045a529

Check Digit Verification of cas no

The CAS Registry Mumber 596-31-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,9 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 596-31:
(5*5)+(4*9)+(3*6)+(2*3)+(1*1)=86
86 % 10 = 6
So 596-31-6 is a valid CAS Registry Number.
InChI:InChI=1/C20H18O/c1-21-20(17-11-5-2-6-12-17,18-13-7-3-8-14-18)19-15-9-4-10-16-19/h2-16H,1H3

596-31-6SDS

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 [methoxy(diphenyl)methyl]benzene

1.2 Other means of identification

Product number -
Other names Trityl methyl ether

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:596-31-6 SDS

596-31-6Relevant articles and documents

Photoactivatable aggregation-induced emission of triphenylmethanol

Zheng, Yue,Zheng, Xiaokun,Xiang, Yu,Tong, Aijun

, p. 11130 - 11133 (2017)

Triphenylmethanol (TPOH) is a non-fluorescent compound. Interestingly, after UV irradiation at 254 nm, TPOH showed a strong blue fluorescence on a solid surface. Moreover, the fluorescence can be quenched by UV irradiation at 365 nm, making the photoactiv

On the Mechanism of the Cleavage Reaction of (Methylthio)methyl Ether with Triphenylmethyl Cation

Niwa, Haruki,Miyachi, Yasuyoshi

, p. 716 - 718 (1991)

The cleavage reaction of a (methylthio)methyl (MTM) ether with triphenylmethyl cation was not initiated by the previously proposed hydride abstraction with triphenylmethyl cation but promoted by the coordination of triphenylmethyl cation as a Lewis acid to the sulfur atom in the MTM group.

Selective reaction of benzyl alcohols with HI gas: Iodination, reduction, and indane ring formations

Matsumoto, Shoji,Naito, Masafumi,Oseki, Takehisa,Akazome, Motohiro,Otani, Yasuhiko

, p. 7254 - 7259 (2017/11/24)

Reactions of benzyl alcohols with HI in solvent-free conditions were examined. Three types of reactions (iodination, reduction, and ring formation) occurred depending on the degree of crowding around the benzyl position and the benzylic stabilization of substrates. Results also showed that the ring formation to give indanes proceeded efficiently when HI was used, and that compounds with electron-rich aromatic rings gave indane derivatives in good yields.

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