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306747-98-8

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306747-98-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 306747-98-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,6,7,4 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 306747-98:
(8*3)+(7*0)+(6*6)+(5*7)+(4*4)+(3*7)+(2*9)+(1*8)=158
158 % 10 = 8
So 306747-98-8 is a valid CAS Registry Number.

306747-98-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-dimethyl-4-(ethylamino)methylpyrazole

1.2 Other means of identification

Product number -
Other names (3,5-Dimethyl-1H-pyrazol-4-ylmethyl)-ethyl-amine

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:306747-98-8 SDS

306747-98-8Downstream Products

306747-98-8Relevant articles and documents

Synthesis and reactivity of 3,5-dimethyl-4-aminomethylpyrazole ligands. An entry to new water-soluble pyrazolate rhodium(I) complexes

Esquius, Glòria,Pons, Josefina,Yá?ez, Ramón,Ros, Josep,Solans, Xavier,Font-Bardía, Mercè

, p. 226 - 233 (2007/10/03)

The new pyrazoles 3,5-dimethyl-4-(ethylamino)methylpyrazole (HL1) and 3,5-dimethyl-4-(isopropylamino)methylpyrazole (HL2), both containing aminoalkyl groups at position 4 have been prepared by aminoalkylation of 3,5-dimethylpyrazole and by the reaction between 1-chloromethyl-3,5-dimethylpyrazolium chloride and NH2R amines. The reaction between HL1, HL2 and [RhCl(COD)]2 resulted in complexes of formula [Rh2(HL1)2(COD)2]Cl2 (1) and [Rh2(HL2)2(COD)2]Cl2 (2), which contained the pyrazole ligands in the 'zwitterionic' pyrazolate-ammonium forms. The X-ray structure analysis of 2 confirmed the neutral nature of bridging-pyrazolate ligands and revealed that 1 and 2 belonged to the [Rh2(Pz)2L2] family of compounds. The same reaction with two equivalents of NaOMe resulted in neutral pyrazolate complexes [Rh2(L1)2(COD)2] (5) and [Rh2(L2)2(COD)2] (6). The reaction between both cationic and neutral pyrazolate complexes and a 1:1 CO-H2 mixture (20 atm) led to the dinuclear pyrazolate-bridged tetracarbonyl compounds 3, 4, 7 and 8 in good yields. Tetracarbonyl complexes 3 and 4 were not isolated in pure state. All the complexes synthesized are soluble in polar solvents such as water.

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