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(S)-N-Boc-3-Methylmorpholine is a chemical compound with a molecular formula of C9H17NO3 and a molecular weight of 187.24 g/mol. It is a derivative of morpholine, containing a Boc (tert-butoxycarbonyl) protecting group and a methyl group attached to the third carbon atom. (S)-N-Boc-3-Methylmorpholine is known for its role as a building block in organic synthesis and drug development, and it has been utilized in the preparation of various pharmaceutical and agrochemical products. Its potential as a chiral base in asymmetric catalysis and as a reactant in the formation of heterocyclic compounds makes it a valuable tool for researchers in the fields of medicinal chemistry and organic chemistry.

1022094-01-4

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1022094-01-4 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
(S)-N-Boc-3-Methylmorpholine is used as a building block for the synthesis of various pharmaceutical and agrochemical products. Its unique structure and functional groups contribute to the development of new and effective compounds with specific therapeutic or pesticidal properties.
Used in Organic Synthesis:
(S)-N-Boc-3-Methylmorpholine is used as a versatile intermediate in organic synthesis. Its Boc protecting group can be selectively removed under mild conditions, allowing for the introduction of other functional groups or further reactions. This makes it a valuable component in the synthesis of complex organic molecules.
Used in Asymmetric Catalysis:
(S)-N-Boc-3-Methylmorpholine is used as a chiral base in asymmetric catalysis. Its stereochemistry can be exploited to induce enantioselectivity in various catalytic reactions, leading to the formation of enantiomerically pure products. This is particularly important in the synthesis of chiral pharmaceuticals and agrochemicals.
Used in the Formation of Heterocyclic Compounds:
(S)-N-Boc-3-Methylmorpholine is used as a reactant in the formation of heterocyclic compounds. Its ability to participate in various cyclization reactions allows for the synthesis of a wide range of heterocyclic structures, which are often found in biologically active molecules and have potential applications in medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 1022094-01-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,2,0,9 and 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1022094-01:
(9*1)+(8*0)+(7*2)+(6*2)+(5*0)+(4*9)+(3*4)+(2*0)+(1*1)=84
84 % 10 = 4
So 1022094-01-4 is a valid CAS Registry Number.

1022094-01-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-N-Boc-3-Methylmorpholine

1.2 Other means of identification

Product number -
Other names (S)-N-Boc-3-Methylmorpholin

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:1022094-01-4 SDS

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