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Bis(2-methoxyphenyl)(phenyl)methanol is an organic compound with the molecular formula C20H20O3. It is a derivative of benzene, featuring two methoxyphenyl groups and one phenyl group attached to a central methanol moiety. bis(2-methoxyphenyl)(phenyl)methanol is characterized by its symmetrical structure and the presence of two methoxy groups, which contribute to its unique chemical properties. It is often used in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals due to its versatile functional groups and potential for further chemical modification. The compound's stability and reactivity make it a valuable intermediate in organic synthesis, particularly in the preparation of complex molecules with potential applications in various industries.

6333-10-4

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6333-10-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6333-10-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,3 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6333-10:
(6*6)+(5*3)+(4*3)+(3*3)+(2*1)+(1*0)=74
74 % 10 = 4
So 6333-10-4 is a valid CAS Registry Number.

6333-10-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name bis(2-methoxyphenyl)-phenylmethanol

1.2 Other means of identification

Product number -
Other names 2.2'-Dimethoxy-tritanol

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:6333-10-4 SDS

6333-10-4Relevant academic research and scientific papers

Access to Enantiopure Triarylmethanes and 1,1-Diarylalkanes by NHC-Catalyzed Acylative Desymmetrization

Lu, Shenci,Song, Xiaoxiao,Poh, Si Bei,Yang, Hui,Wong, Ming Wah,Zhao, Yu

supporting information, p. 2275 - 2281 (2017/02/23)

We present herein an unprecedented, efficient and enantioselective synthesis of triarylmethanes and 1,1-diarylalkanes through N-heterocyclic carbene-catalyzed acylative desymmetrization of bisphenols. This method utilizes readily available substrates, reagents and a simple procedure to deliver the valuable products in excellent enantiopurity. DFT calculations reveal that the selectivity is governed by the C?C bond cleavage step of the tetrahedral intermediate leading to the ester product. A transition state model featuring a combination of intramolecular hydrogen bond and steric effect is developed to explain the enantioselectivity.

Phosphotriester oligonucleotides, amidites and method of preparation

-

, (2008/06/13)

Oligonucleotides having bioreversible phosphate blocking groups can be used as pro drugs for the oligonucleotides. The bio-reversible blocking groups can be removed by intercellular enzymes, particularly carboxyesterases, to provide the unprotected oligonucleotide. The oligonucleotides can be prepared via post synthesis alkylation reactions or utilizing amidite type chemistry wherein the bioreversible phosphorus protecting group is formed as an integral part of the amidite reagent.

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