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2,5-dioxooxazolidine-4-acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16875-31-3

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16875-31-3 Usage

Type

Carbonic anhydrase inhibitor

Uses

Treatment of glaucoma, epilepsy, and altitude sickness

Mechanism (glaucoma)

Reduces production of aqueous humor in the eye, lowering intraocular pressure and relieving symptoms of glaucoma

Mechanism (epilepsy)

Inhibits the enzyme carbonic anhydrase, reducing abnormal electrical discharges in the brain that lead to seizures

Mechanism (altitude sickness)

Decreases symptoms of dizziness, headache, nausea, and shortness of breath experienced at high altitudes

Other use

As a diuretic to increase urine production and treat fluid retention

Importance

Has a wide range of medical applications and is an important medication in various therapeutic areas.

Check Digit Verification of cas no

The CAS Registry Mumber 16875-31-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,8,7 and 5 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 16875-31:
(7*1)+(6*6)+(5*8)+(4*7)+(3*5)+(2*3)+(1*1)=133
133 % 10 = 3
So 16875-31-3 is a valid CAS Registry Number.
InChI:InChI=1/C5H6N2O4/c6-3(8)1-2-4(9)11-5(10)7-2/h2H,1H2,(H2,6,8)(H,7,10)

16875-31-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2,5-dioxo-1,3-oxazolidin-4-yl)acetamide

1.2 Other means of identification

Product number -
Other names EINECS 240-908-6

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:16875-31-3 SDS

16875-31-3Downstream Products

16875-31-3Relevant academic research and scientific papers

ENANTIOMERIC QUANTIFICATIONS OF AMINO ACIDS THROUGH THEIR Nα-ACYL AMIDES BY GAS CHROMATOGRAPHY.

Hosten, N.,Anteunis, M. J. O.

, p. 45 - 47 (2007/10/02)

Apparent separation of 1.1 or higher on Chiralsil Val III can be obtained for Nα-acyl N-alkyl aminoacid amides allowing the use of short capillary gas chromatographic columns.A clean derivatization protocol without racemization is described, proceding through the NCA derivatives that are prepared from "in situ" silylated amino acids with trimethylsilyl cyanide.

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