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29817-47-8

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29817-47-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29817-47-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,8,1 and 7 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 29817-47:
(7*2)+(6*9)+(5*8)+(4*1)+(3*7)+(2*4)+(1*7)=148
148 % 10 = 8
So 29817-47-8 is a valid CAS Registry Number.

29817-47-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-dihydroxyadamantane diacetate

1.2 Other means of identification

Product number -
Other names 1,3-Diacetoxyadamantan

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:29817-47-8 SDS

29817-47-8Downstream Products

29817-47-8Relevant articles and documents

Polarized C-H Groups as Novel Hydrogen-Bond Donors in Hydryl-F-alkyl Esters: Unequivocal Examples for the "Pinchas Effect"

Adcock, James L.,Zhang, Huqiu

, p. 1999 - 2002 (1995)

1H NMR and IR spectral evidence for a C-H...O hydrogen bonds in 1- trifluoroacetate and 1,3- bis(trifluoroacetate) are presented.Evidence indicating a three-center hydrogen bond in 1,3- bis(trifluoroacetate) is also presented.Both compounds, despite otherwise normal 1H NMR chemical shift displacements and carbonyl stretching frequency depressions, show strong increases in C-H stretching frequencies related to hydrogen-bond interactions (the "Pinchas Effect").

Process for producing oxygen-bearing compound

-

Page/Page column 5-7, (2008/06/13)

Provided is a process for industrially advantageously producing an oxygen-bearing compound (e.g., an alcohol, a diol, a polyol, or a ketone) through oxidation of an alkane or an alcohol, which process requires no treatment for separation/removal of a catalyst and causes no equipment corrosion. Specifically, there are provided a process for producing an oxygen-bearing compound, including oxidizing an alkane in the presence of a catalyst containing at least one element selected from among transition metal elements belonging to Groups 5 and 8 to 10 of the periodic table, wherein the oxygen-bearing compound is an alcohol, a diol, a polyol, or a ketone; and a process for producing an oxygen-bearing compound, including oxidizing an alcohol in the presence of a catalyst containing at least one element selected from among transition metal elements belonging to Groups 5 and 8 to 10 of the periodic table, wherein the oxygen-bearing compound is a diol, a polyol, or a ketone.

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