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5464-86-8

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5464-86-8 Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 71, p. 2031, 1949 DOI: 10.1021/ja01174a037

Check Digit Verification of cas no

The CAS Registry Mumber 5464-86-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,6 and 4 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5464-86:
(6*5)+(5*4)+(4*6)+(3*4)+(2*8)+(1*6)=108
108 % 10 = 8
So 5464-86-8 is a valid CAS Registry Number.
InChI:InChI=1/C15H16O2/c16-11-15(12-17,13-7-3-1-4-8-13)14-9-5-2-6-10-14/h1-10,16-17H,11-12H2

5464-86-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-diphenylpropane-1,3-diol

1.2 Other means of identification

Product number -
Other names 1,3-Dihydroxy-2,2-diphenyl-propan

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:5464-86-8 SDS

5464-86-8Relevant articles and documents

Asymmetric Conjugate Addition of Alkylzirconocenes to Cyclopent-4-ene-1,3-dione Monoacetals

Rideau, Emeline,M?sing, Florian,Fletcher, Stephen P.

supporting information, p. 2217 - 2222 (2015/08/03)

Copper-catalyzed asymmetric conjugate additions are powerful reactions that allow the formation of single-enantiomer building blocks in a few steps. However, highly enantioselective conjugate addition to five-membered-ring substrates is more challenging a

Platinum-catalyzed cycloisomerization of 1,4-enynes via 1,2-alkenyl rearrangement

Sato, Takuma,Onuma, Toshiki,Nakamura, Itaru,Terada, Masahiro

supporting information; experimental part, p. 4992 - 4995 (2011/11/14)

The cycloisomerization of 1,4-enyne 1 in the presence of platinum(II) catalyst afforded 1,2,3-trisubstituted 1H-indene 2 and 20 in good to excellent yields. The reaction proceeded through an unprecedented 1,2-alkenyl rearrangement that afforded a novel re

Diethers usable in the preparation of Ziegler-Natta catalysts and their preparation

-

, (2008/06/13)

Diethers of general formula: where R, RI, RII, RIII, RIVand RV, same or different, are H or linear or branched alkyl, cycloalkyl, aryl, alkylaryl or arylalkyl radicals with 1-18 carbon atoms, provided that R and RIare not both H or CH3 or are not CH3 and n-propyl; RVIand RVIIthe same or different, are linear or branched alkyl, cycloaliphatic, aryl, or arylalkyl radicals having 1-18 carbon atoms; one or more of R to RVIImay be bonded to form a cyclic structure. The diethers are particularly useful in the preparation of Ziegler-Natta catalysts.

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