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1H-Pyrazole-3-carboxylic acid, 1-acetyl-4,5-dihydro-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

49846-69-7

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49846-69-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 49846-69-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,8,4 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 49846-69:
(7*4)+(6*9)+(5*8)+(4*4)+(3*6)+(2*6)+(1*9)=177
177 % 10 = 7
So 49846-69-7 is a valid CAS Registry Number.

49846-69-7SDS

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 1-acetyl-3-methoxycarbonyl-2-pyrazoline

1.2 Other means of identification

Product number -
Other names 1-acetyl-4,5-dihydro-1H-pyrazole-3-carboxylic acid methyl ester

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:49846-69-7 SDS

49846-69-7Downstream Products

49846-69-7Relevant academic research and scientific papers

N,N'-LINKED BIAZOLES. PART 5. SYNTHESIS OF PYRAZOLYL DIMERS BY THE REACTION OF 3-METHOXYCARBONYL-2-PYRAZOLINE WITH LEAD TETRAACETATE

Mendoza, Javier de,Gonzales-Muniz, M. Rosario,Martin, M. Rosario,Elguero, Jose

, p. 2619 - 2628 (2007/10/02)

Contrary to a previous report by Akhrem et. al. (Tetrahedron Lett. 1973, 2655), the reaction of 3-methoxycarbonyl-2-pyrazoline with lead tetraacetate affords not only 3-methoxycarbonyl-1-(3-methoxycarbonyl-2-pyrazolin-1-yl)pyrazole (8) and 3-methoxycarbonyl-1-(1-methoxycarbonyl-1-cyclopropyl)pyrazole (9), but a complex mixture of pyrazoles and pyrazolines depending on the reaction conditions (LTA/pyrazoline ratio and temperature).The structures of all compounds have been established, and a new mechanism is proposed for the reaction.The oxidation of 8 with N-bromosuccinimide gave the symmetrical 3,3'-dimethoxycarbonyl-1,1'-bipyrazole (17).

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