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2-Oxazolamine,4,5-dihydro-5-methyl-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

68210-19-5

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68210-19-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68210-19-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,2,1 and 0 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 68210-19:
(7*6)+(6*8)+(5*2)+(4*1)+(3*0)+(2*1)+(1*9)=115
115 % 10 = 5
So 68210-19-5 is a valid CAS Registry Number.

68210-19-5SDS

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 5-methyl-4,5-dihydro-oxazol-2-ylamine

1.2 Other means of identification

Product number -
Other names 2-Imino-5-methyl-1.3-oxazolidin

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:68210-19-5 SDS

68210-19-5Downstream Products

68210-19-5Relevant academic research and scientific papers

4,5-Disubstituted-1,3-oxazolidin-2-imine derivatives: A new class of orally bioavailable nitric oxide synthase inhibitor

Ueda, Shigeo,Terauchi, Hideo,Yano, Akihiro,Ido, Motoharu,Matsumoto, Masashi,Kawasaki, Motoji

, p. 313 - 316 (2007/10/03)

In our search for a novel class of inducible nitric oxide synthase (iNOS) inhibitors, 1,3-oxazolidin-2-imine was found to weakly inhibit iNOS. Further modifications of this compound resulted in a remarkable increase in both the in vivo and in vitro inhibi

An efficient synthesis of a new series of acyclonucleosides starting from β-amino alcohols

Agami, Claude,Dechoux, Luc,Hamon, Louis,Melaimi, Mohand

, p. 6666 - 6669 (2007/10/03)

A series of new acyclonucleosides analogues 3 has been synthesized very efficiently in three steps starting from β-amino alcohols 1. The key step of this process is a nucleophilic substitution with various nucleophiles on 2,2'-anhydronucleosides 2. The chemo- and stereoselectivities of this reaction are discussed. AM1 calculations sustained the observed chemoselectivity.

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