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84772-29-2

84772-29-2

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  • China Largest Manufacturer factory sales L-Ornithine ethylester dihydrochloride CAS 84772-29-2

    Cas No: 84772-29-2

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84772-29-2 Usage

Chemical Properties

Snow white (hygroscopic)

Check Digit Verification of cas no

The CAS Registry Mumber 84772-29-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,7,7 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 84772-29:
(7*8)+(6*4)+(5*7)+(4*7)+(3*2)+(2*2)+(1*9)=162
162 % 10 = 2
So 84772-29-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H16N2O2.2ClH/c1-2-11-7(10)6(9)4-3-5-8;;/h6H,2-5,8-9H2,1H3;2*1H/t6-;;/m0../s1

84772-29-2SDS

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 ethyl (2S)-2,5-diaminopentanoate,dihydrochloride

1.2 Other means of identification

Product number -
Other names L-Ornithine Ethyl ester Dihydrochloride

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:84772-29-2 SDS

84772-29-2Relevant articles and documents

Diastereoselective pictet-spengler reactions of a tethered 2-aminoimidazole

Shengule, Sudhir R.,Karuso, Peter

, p. 184 - 191 (2014/03/21)

The diastereoselective Pictet-Spengler reaction of aminopropyl-2- aminoimidazole with enantiopure aldehydes has been investigated. With amino acid-derived aldehydes, anti stereochemistry is favoured, with a diastereoselectivity up to 92% achievable. The absolute stereochemistry of the products was determined through synthesis of a rigid derivative and from NMR data in combination with molecular modelling. The diastereoselectivity was shown to be dependent on the steric bulk of the amino acid side chain and independent of the nitrogen protecting group. Lewis acids catalysed the reaction but did not affect the diastereoselectivity.

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