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1023-91-2

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1023-91-2 Usage

General Description

1,3-dihydro-3,3-dimethyl-1-phenylisobenzofuran-1-ol is a chemical compound with a complex molecular structure consisting of a benzofuran ring with a phenyl group and a hydroxyl group attached. It is a white solid at room temperature and is soluble in organic solvents such as ethanol and acetone. 1,3-dihydro-3,3-dimethyl-1-phenylisobenzofuran-1-ol is used in the pharmaceutical industry as an intermediate in the synthesis of various drugs and biologically active compounds. It may also have potential applications in the field of organic chemistry as a building block for the construction of more complex molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 1023-91-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,2 and 3 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1023-91:
(6*1)+(5*0)+(4*2)+(3*3)+(2*9)+(1*1)=42
42 % 10 = 2
So 1023-91-2 is a valid CAS Registry Number.
InChI:InChI=1/C16H16O2/c1-15(2)13-10-6-7-11-14(13)16(17,18-15)12-8-4-3-5-9-12/h3-11,17H,1-2H3

1023-91-2SDS

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 3,3-dimethyl-1-phenyl-2-benzofuran-1-ol

1.2 Other means of identification

Product number -
Other names 2-(1-hydroxy-1-methyl-ethyl)-benzophenone cyclohemiacetal

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:1023-91-2 SDS

1023-91-2Relevant articles and documents

Free energy and entropy changes in vertical and nonvertical triplet energy transfer processes between rigid and nonrigid molecules. A laser photolysis study

Zhang, Daisy,Closs, Gerhard L.,Chung, Dutch D.,Norris, James R.

, p. 3670 - 3673 (1993)

The free energy and entropy changes associated with intermolecular triplet energy transfer (TT) processes were determined by direct measurement of the equilibrium constant using a laser flash photolysis technique. 10,10-Dimethylanthrone and 9,9-dimethylfluorene were synthesized and used as a "rigid" donor and acceptor, respectively, in comparison with 4-methylbenzophenone, a "nonrigid" donor, and 4-methylbiphenyl, a "nonrigid" acceptor, in the TT reactions. Both the nonrigid donor and the nonrigid acceptor lose entropy while going from the twisted ground state to the planar triplet state. The ΔS values for 4-methylbenzophenone and 4-methylbiphenyl are 0.5-1.0 and 2.5-3.0 gibbs/mol, respectively.

Preparation method of 10,10-dimethylanthrone

-

Paragraph 0021; 0023; 0025; 0027; 0029; 0031, (2019/06/30)

The invention belongs to the field of drug synthesis and provides a novel method of synthesizing melitracen hydrochloride intermediate 10,10-dimethylanthrone. The 10,10-dimethylanthrone is prepared from phthalic anhydride as a start material through two-step Grignard reaction and three-step closed-ring reaction. The total yield is up to 30%, and the purity of the finished intermediate is higher than 98.0%. Compared with traditional synthetic processes, the novel process herein has simple steps and greatly reduced production cost, causes little environmental pollution and helps greatly solve the environmental issue caused by the production of 10,10-dimethylanthrone.

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