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5919-84-6

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5919-84-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5919-84-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,1 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5919-84:
(6*5)+(5*9)+(4*1)+(3*9)+(2*8)+(1*4)=126
126 % 10 = 6
So 5919-84-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H18O3/c1-7(2)8(11)12-6-9(3,4)5-10/h7,10H,5-6H2,1-4H3

5919-84-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-hydroxy-2,2-dimethylpropyl) 2-methylpropanoate

1.2 Other means of identification

Product number -
Other names isobutyric acid neopentyl glycol monoester

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:5919-84-6 SDS

5919-84-6Downstream Products

5919-84-6Relevant articles and documents

Retention Indices and Enthalpies of Sorption of Esters of Neopentyl Glycol on DB-1 Stationary Phase

Krasnykh, E. L.,Levanova, S. V.,Lukina, O. D.,Portnova, S. V.

, p. 659 - 661 (2020/04/15)

Abstract: The logarithmic retention indices and the enthalpies of sorption at the average temperature of an experiment and 298.2 K are determined via gas–liquid chromatography using DB-1 stationary phase for esters of neopentyl glycol and С2–С

EXTERNALLY MASKED NEOPENTYL SULFONYL ESTER CYCLIZATION RELEASE PRODRUGS OF ACAMPROSATE, COMPOSITIONS THEREOF, AND METHODS OF USE

-

Page/Page column 44-45, (2009/04/24)

Masked nitrogen-substituted and oxygen-substituted neopentyl sulfonyl ester prodrugs of acamprosate, pharmaceutical compositions comprising such prodrugs, and methods of using such prodrugs and compositions thereof for treating diseases are disclosed. In particular, acamprosate prodrugs exhibiting enhanced oral bioavailability and methods of using acamprosate prodrugs to treat neurodegenerative disorders, psychotic disorders, mood disorders, anxiety disorders, somatoform disorders, movement disorders, substance abuse disorders, binge eating disorder, cortical spreading depression related disorders, tinnitus, sleeping disorders, multiple sclerosis, and pain are disclosed.

Stabilized hydroxypivalaldehyde

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

In the method of the invention, hydroxypivalaldehyde (3-hydroxy-2,2-dimethylpropanal) and/or its dimer is stored under solid conditions containing an amount of water. By storing such solid conditions, hydroxypivalaldehyde and/or its dimer is stored for a long period of time without reducing its purity.

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