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26562-81-2

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26562-81-2 Usage

Purification Methods

Dissolve it in boiling conc HCl (400mg in 15mL) and evaporate to dryness. Dissolve it in absolute EtOH and add dry Et2O to crystallise the dihydrochloride. [Stetter & Wulff Chem Ber 93 1366 1960, Beilstein 13 III 27,]

Check Digit Verification of cas no

The CAS Registry Mumber 26562-81-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,5,6 and 2 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 26562-81:
(7*2)+(6*6)+(5*5)+(4*6)+(3*2)+(2*8)+(1*1)=122
122 % 10 = 2
So 26562-81-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H18N2.2ClH/c11-9-2-7-1-8(4-9)5-10(12,3-7)6-9;;/h7-8H,1-6,11-12H2;2*1H

26562-81-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name adamantane-1,3-diamine,dihydrochloride

1.2 Other means of identification

Product number -
Other names adamantane-1,3-diamine 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:26562-81-2 SDS

26562-81-2Relevant articles and documents

Synthesis of diacetylamino and diamino derivatives of adamantane series

Klimochkin, Yu. N.,Ivleva,Serzhantova,Shiryaev,Moiseev

, p. 1170 - 1175 (2017)

1,3-Diacetylamino derivatives were synthesized directly from adamantane series hydrocarbons or from adamantan-1-ylacetic acids by a one-pot method with a succession of an oxidation stage and Ritter’s reaction in nitric acid and in a mixture of sulfuric and nitric acids. The hydrolysis of 1,3-diacetylamino derivatives in an acidic medium leads to scaffold diamines and diaminoacids.

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