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26314-06-7

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26314-06-7 Usage

General Description

2,5-Oxazolidinedione, 4,4-diphenyl- is a chemical compound commonly known as DPH. It is a white crystalline solid that is insoluble in water and has a faint odor. DPH is primarily used as a cross-linking agent in polymer chemistry, especially in the production of epoxy resins and polyurethanes. It is also used as a curing agent for epoxy resins and as a flame-retardant in some plastic materials. DPH is considered to be a skin and eye irritant and may cause respiratory irritation if inhaled. It is important to handle and store this chemical with proper safety precautions.

Check Digit Verification of cas no

The CAS Registry Mumber 26314-06-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,3,1 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 26314-06:
(7*2)+(6*6)+(5*3)+(4*1)+(3*4)+(2*0)+(1*6)=87
87 % 10 = 7
So 26314-06-7 is a valid CAS Registry Number.
InChI:InChI=1/C15H11NO3/c17-13-15(16-14(18)19-13,11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10H,(H,16,18)

26314-06-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,4-diphenyl-1,3-oxazolidine-2,5-dione

1.2 Other means of identification

Product number -
Other names 4,4-Diphenyl-oxazolidin-2,5-dion

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:26314-06-7 SDS

26314-06-7Relevant articles and documents

Synthesis of sterically hindered N-acylated amino acids from N-carboxyanhydrides

Schaefer, Gabriel,Bode, Jeffrey W.

supporting information, p. 1526 - 1529 (2014/04/03)

Sterically hindered N-acyl, gem-disubstituted amino acids are easily prepared via the addition of organometallic reagents to N-carboxyanhydrides (NCA). The process tolerates a wide variety of functional groups and allows the synthesis of amide products not readily accessible by traditional acylation chemistry. The existence of an isocyanate intermediate was established by in situ IR spectroscopy.

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