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Pyridine, 3,5-dimethyl-2-(1-methyl-1-butenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

37108-99-9

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37108-99-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37108-99-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,1,0 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 37108-99:
(7*3)+(6*7)+(5*1)+(4*0)+(3*8)+(2*9)+(1*9)=119
119 % 10 = 9
So 37108-99-9 is a valid CAS Registry Number.

37108-99-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(α-methylbuten-1-yl)-3,5-dimethylpyridine

1.2 Other means of identification

Product number -
Other names -

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:37108-99-9 SDS

37108-99-9Downstream Products

37108-99-9Relevant academic research and scientific papers

SYNTHESIS OF ALKYL-SUBSTITUTED PYRIDINES FROM CO, C2H4, H2, and NH3 ON HETEROGENEOUS CATALYSTS

Kosolapova, B. S.,Levin, D. Z.,Sominskii, S. D.,Rar, L. F.,Mortikov, E. S.,Lapidus, A. L.

, p. 2244 - 2248 (2007/10/02)

The reaction of preparation of alkyl-substituted pyridines by hydroformylation of ethylene in the presence of ammonia on heterogeneous Rh-containing catalysts with the formation of 2-ethyl-3,5-dimethylpyridine (I) as the basic product with up to 70-80percent conversion of gases and up to an 80 wt. percent concentration of the basic product was investigated.The dependence of the activity and selectivity of the catalysts on the concentration of Rh and nature of the support was determined.A correlation between the activity of the catalysts and their acid properties was established by IR spectroscopy.

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