34671-29-9 Usage
Uses
Used in Pharmaceutical Synthesis:
2-Iodo-1-methylpyrrole is used as a key intermediate for the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in Chemical Compounds Production:
2-Iodo-1-methylpyrrole is utilized as a reagent in organic chemistry reactions, playing a crucial role in the production of a wide range of chemical compounds.
Used in Agrochemicals Production:
2-Iodo-1-methylpyrrole is used as a precursor in the production of agrochemicals, aiding in the development of agricultural products that enhance crop protection and yield.
Used in Specialty Chemicals Production:
It serves as an important intermediate in the synthesis of specialty chemicals, which are used in various industries for specific applications.
Used in Organic Electronics and Materials Science:
2-Iodo-1-methylpyrrole has applications in the field of organic electronics and materials science, where it contributes to the advancement of innovative materials and electronic devices.
Check Digit Verification of cas no
The CAS Registry Mumber 34671-29-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,6,7 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 34671-29:
(7*3)+(6*4)+(5*6)+(4*7)+(3*1)+(2*2)+(1*9)=119
119 % 10 = 9
So 34671-29-9 is a valid CAS Registry Number.
34671-29-9Relevant academic research and scientific papers
An improved procedure for the preparation of aryl- and hetarylacetylenes
Mal'Kina,Brandsma,Vasilevsky,Trofimov
, p. 589 - 590 (2007/10/03)
A number of relatively volatile acetylenes RC ≡ CH (R = aryl or hetaryl) have been prepared with high yields by heating a mixture of the corresponding alcohols RC ≡ CC(CH3)2OH and paraffin oil with small amounts of powdered potassium hydroxide in vacuum. The alcohols were obtained by Pd/Cu-catalyzed cross coupling of aryl or hetaryl halides RX (X = Br, in one case I) with the commercially available HC ≡ CC(CH3)2OH.
EFFECT OF HALOGEN ON THE REACTION OF 1-METHYLPYRROLE WITH N-HALOIMIDES.
Rosa, Michael De,Nieto, Gustavo Cabrera
, p. 2405 - 2408 (2007/10/02)
In the reaction of N-haloimides with 1-methylpirrole, ?-substitution (addition-elimination) predominates over halogenation, when the halogen is chlorine.
