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2,2,6,6-Tetramethyltetrahydro-1H,5H-pyrazolo[1,2-a]pyrazole is a complex organic compound with the molecular formula C8H16N2. It is a heterocyclic molecule, featuring a pyrazole ring fused to a pyrazole ring, with two methyl groups attached to each of the carbon atoms at positions 2 and 6. 2,2,6,6-tetramethyltetrahydro-1H,5H-pyrazolo[1,2-a]pyrazole is known for its potential applications in various chemical and pharmaceutical industries, such as a precursor in the synthesis of pharmaceuticals or as a ligand in coordination chemistry. Its unique structure and properties make it an interesting subject for research and development in the field of organic chemistry.

2940-98-9

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2940-98-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2940-98-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,4 and 0 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2940-98:
(6*2)+(5*9)+(4*4)+(3*0)+(2*9)+(1*8)=99
99 % 10 = 9
So 2940-98-9 is a valid CAS Registry Number.

2940-98-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,6,6-tetramethyl-1,3,5,7-tetrahydropyrazolo[1,2-a]pyrazole

1.2 Other means of identification

Product number -
Other names 3,3,7-7-Tetramethyl-1,5-diazabicyclo<3.3.0>octan

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:2940-98-9 SDS

2940-98-9Downstream Products

2940-98-9Relevant academic research and scientific papers

Reduction of β-Lactams,III. Synthesis of β-Thiolactams and Reduction with Raney Nickel

Verkoyen, Carl,Rademacher, Paul

, p. 653 - 660 (2007/10/02)

The N-substituted β-lactams 1-3 react with P2S5 or Lawesson reagent (11) to give the β-thiolactams 5-7.The bi-β-lactam 4 is transformed by 11 to the bi-β-thiolactam 8, with P2S5 however rearrangement occurs to the bicyclic thiohydrazide 10. - Reduction wi

Reduction of β-Lactams, I. Reduction of 3,3,3',3'-Tetramethyl-2,2'-dione with Complex Hydrides

Verkoyen, Carl,Rademacher, Paul

, p. 1659 - 1670 (2007/10/02)

Reduction of the title compound 7 with lithium aluminium hydride leads to four products 8 to 11 in yields depending on the reaction conditions.Compounds 8 to 10 are also obtained from the bicyclic hydrazide 12, isomeric with 7.Therefore, the reduction of 7 and 12 is likely to proceed in part via common intermediates.A reaction scheme is proposed to account for the generation of the products.With other hydride reagents comlex reaction mixtures are obtained from 7.The reduction of 7 to 3,3,3',3'-tetramethyl-1,1'-biazetidine (13) failed.

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