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2-METHYL-4-(METHYLAMINO)BUTAN-2-OL, also known as "diphenylmethyl-(4-methyl-2-propan-2-yl-1,3-oxazolidin-2-yl)methanol", is a chemical compound with the molecular formula C7H17NO. It is a viscous liquid at room temperature and is soluble in water. 2-METHYL-4-(METHYLAMINO)BUTAN-2-OL is commonly used as a pharmaceutical intermediate and organic building block, and can be produced through a multi-step synthetic process involving several chemical reactions.

866223-53-2

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866223-53-2 Usage

Uses

Used in Pharmaceutical Industry:
2-METHYL-4-(METHYLAMINO)BUTAN-2-OL is used as a pharmaceutical intermediate for the synthesis of various pharmaceuticals and organic compounds. Its unique chemical structure and properties make it a valuable component in the development of new drugs and medications.
Used in Chemical Industry:
2-METHYL-4-(METHYLAMINO)BUTAN-2-OL is also used as an organic building block in the chemical industry. Its versatility and solubility in water make it a useful component in the synthesis of a wide range of organic compounds for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 866223-53-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,6,2,2 and 3 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 866223-53:
(8*8)+(7*6)+(6*6)+(5*2)+(4*2)+(3*3)+(2*5)+(1*3)=182
182 % 10 = 2
So 866223-53-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H15NO/c1-6(2,8)4-5-7-3/h7-8H,4-5H2,1-3H3

866223-53-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Methyl-4-(MethylaMino)butan-2-ol

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

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More Details:866223-53-2 SDS

866223-53-2Downstream Products

866223-53-2Relevant academic research and scientific papers

Carbanion-accelerated claisen rearrangements: Asymmetric induction with chiral phosphorus-stabilized anions

Denmark, Scott E.,Marlin, John E.,Rajendra

, p. 66 - 82 (2013)

The carbanion-accelerated Claisen rearrangement has been extended to include phosphorus carbanion-stabilizing groups. The appropriately substituted allyl vinyl ethers are synthesized by the nucleophilic addition of allyl oxides to phosphorus-substituted allenes, which are obtained in one step from simple starting materials. The phosphorus-stabilized, carbanion-accelerated Claisen rearrangements proceed rapidly at room temperature in high yield, and the rearrangements are highly site- and stereoselective. The first examples of asymmetric induction in the Claisen rearrangement with chiral, phosphorus, anion-stabilizing groups are described. The observed asymmetric induction is highly dependent on the structure of the auxiliary and the metal counterion involved. Both internal and relative diastereoselectivity are high. A model for the observed sense of internal diastereoselectivity is proposed that is founded in the current understanding of the structure of phosphorus-stabilized anions.

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