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38614-36-7 Usage

Chemical Properties

Yellow to dark orange liquid


Different sources of media describe the Uses of 38614-36-7 differently. You can refer to the following data:
1. 2-Methyl-1-propenylmagnesium bromide(0.5?M in THF) is a reagent used in many chemical reactions such as in the preparation of biaryls, alkylarenes, alkenylarenes, alkynylalkenones via nucleophilic addition.Used in the study of palladium-catalyzed coupling with aryl tosylates.
2. Used in a synthesis of (2S,3S)-3′-fluoroisoleucine.
3. 2-Methyl-1-propenylmagnesium bromide can be used in a study of a palladium-catalyzed coupling with aryl tosylates.

Check Digit Verification of cas no

The CAS Registry Mumber 38614-36-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,6,1 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 38614-36:
127 % 10 = 7
So 38614-36-7 is a valid CAS Registry Number.

38614-36-7 Well-known Company Product Price

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  • CAS number
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  • Aldrich

  • (419613)  2-Methyl-1-propenylmagnesiumbromidesolution  0.5 M in THF

  • 38614-36-7

  • 419613-100ML

  • 1,535.04CNY

  • Detail
  • Aldrich

  • (419613)  2-Methyl-1-propenylmagnesiumbromidesolution  0.5 M in THF

  • 38614-36-7

  • 419613-800ML

  • 4,656.60CNY

  • Detail

38614-36-7Relevant articles and documents

Broadly Applicable Stereoselective Syntheses of Serrulatane, Amphilectane Diterpenes, and Their Diastereoisomeric Congeners Using Asymmetric Hydrovinylation for Absolute Stereochemical Control

Tenneti, Srinivasarao,Biswas, Souvagya,Cox, Glen Adam,Mans, Daniel J.,Lim, Hwan Jung,RajanBabu

supporting information, p. 9868 - 9881 (2018/07/25)

A stereogenic center, placed at an exocyclic location next to a chiral carbon in a ring to which it is attached, is a ubiquitous structural motif seen in many bioactive natural products, including di- and triterpenes and steroids. Installation of these ce

Bridgehead Reactivity, Nucleophilic and Radical Additions, and Lithium Aluminum Hydride Reduction of 1-(Arylsulfonyl)bicyclobutanes: General Access to Substituted, Functionalized Cyclobutanes. Syntheses of (+/-)-Citrilol Acetate, (+/-)-Junionone, and the

Gaoni, Yehiel,Tomazic, Alenka

, p. 2948 - 2957 (2007/10/02)

A general approach to the synthesis of a wide range of substituted cyclobutane derivatives is based on two specific reactions of 1-(arylsulfonyl)bicyclobutanes (1) and on some general reactions of the bicyclobutane ring systems.One specific cyclobutane fo

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