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59772-30-4

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59772-30-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59772-30-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,7,7 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 59772-30:
(7*5)+(6*9)+(5*7)+(4*7)+(3*2)+(2*3)+(1*0)=164
164 % 10 = 4
So 59772-30-4 is a valid CAS Registry Number.

59772-30-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (4,5-dihydro-1H-imidazol-2-yl)-(2-ethyl-6-methyl-phenyl)-amine

1.2 Other means of identification

Product number -
Other names 2-(2-Ethyl-6-methylphenylimino)-imidazolidin

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:59772-30-4 SDS

59772-30-4Downstream Products

59772-30-4Relevant articles and documents

Three-dimensional common-feature hypotheses for octopamine agonist 2-(arylimino)imidazolidines

Hirashima, Akinori,Morimoto, Masako,Kuwano, Eiichi,Taniguchi, Eiji,Eto, Morifusa

, p. 117 - 123 (2007/10/03)

Three-dimensional pharmacophore hypotheses were built from a set of 10 octopamine (OA) agonist 2-(Arylimino)imidazolidines (AIIs), 2-(Arylimino)thiazolidines (AITs) and 2-(Arylimino)oxazolidines (AIOs). Among the 10 common-featured models generated by program Catalyst/HipHop, a hypothesis including a ring aromatic (RA), a positive ionizable (PI) and three hydrophobic aliphatic (HpA1) features was considered to be important in evaluating the OA-agonist activity. Active OA agonist 2,6-Et2 AII mapped well onto all the RA, PI and HpAl features of the hypothesis. On the other hand, less active compounds were shown to be difficult to achieve the energetically favorable conformation which is found in the active molecules in order to fit the 3-D common-feature pharmacophore models. Taken together, 2,6-Et2-Ph and foramidine structures are important as OA agonists. The present studies on OA agonists demonstrate that a RA, a PI and three HpAl sites located on the molecule seem to be essential for OA-agonist activity. Copyright

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