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26849-62-7

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26849-62-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26849-62-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,8,4 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 26849-62:
(7*2)+(6*6)+(5*8)+(4*4)+(3*9)+(2*6)+(1*2)=147
147 % 10 = 7
So 26849-62-7 is a valid CAS Registry Number.

26849-62-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl cis-2-amino-1-cyclohexanecarboxylate

1.2 Other means of identification

Product number -
Other names ethyl cis-2-aminocyclohexane-1-carboxylate

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:26849-62-7 SDS

26849-62-7Relevant articles and documents

Derivative of hyaluronic acid modified with amino-carboxylic acid

-

, (2016/02/12)

The present invention provides a hyaluronic acid derivative comprising disaccharide units of Formula (I), and a hyaluronic acid derivative/drug conjugate wherein one or more drugs are conjugated to the hyaluronic acid derivative.

Regio- and stereoselective reactions between cyclic Baylis-Hillman type adducts and N-nucleophiles and P-nucleophile

Krawczyk, Ewa,Owsianik, Krzysztof,Skowrońska, Aleksandra

, p. 1449 - 1457 (2007/10/03)

New important organic compounds multifunctionalized cyclic 6-membered and 7-membered allylic amines, azide and phosphonates have been obtained via regio- and diastereoselective reactions of cyclic Baylis-Hillman type adducts 1 with N-nucleophiles and P-nu

Diastereo and Enantioselective Entry to β-Amino Esters by Hydride Reduction of Homochiral β-Enamino Esters.

Cimarelli, Cristina,Palmieri, Gianni,Bartoli, Giuseppe

, p. 1455 - 1458 (2007/10/02)

The reduction of homochiral β-enamino esters 1 with sodium triacetoxyborohydride, which occurs with good diastereo- and enantioselectivity in the β-amino esters 2, is described.The procedure allows a straightforward preparation of compounds with known bio

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