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((2R,6S)-4-benzyl-6-(benzyloxymethyl)morpholin-2-yl)methanol is a morpholine derivative characterized by a benzyl group and an oxymethyl group attached to the morpholine ring. It possesses a specific stereochemistry with the 2R and 6S configuration, which contributes to its unique structure and potential pharmaceutical properties. ((2R,6S)-4-benzyl-6-(benzyloxymethyl)morpholin-2-yl)methanol holds promise for applications in organic synthesis and medicinal chemistry, making it a subject of interest for future research and development.

1093085-89-2

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1093085-89-2 Usage

Uses

Used in Organic Synthesis:
((2R,6S)-4-benzyl-6-(benzyloxymethyl)morpholin-2-yl)methanol is used as a building block in organic synthesis for its unique structural features, which can be utilized to create a variety of complex organic molecules with potential applications in different industries.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, ((2R,6S)-4-benzyl-6-(benzyloxymethyl)morpholin-2-yl)methanol is used as a potential pharmaceutical agent due to its unique structure and properties. Its specific stereochemistry may contribute to its interaction with biological targets, making it a candidate for the development of new drugs.
Used in Pharmaceutical Industry:
((2R,6S)-4-benzyl-6-(benzyloxymethyl)morpholin-2-yl)methanol is used as a precursor in the synthesis of pharmaceutical compounds. Its unique structural features and potential pharmaceutical properties make it a valuable component in the development of new medications.
Used in Research and Development:
((2R,6S)-4-benzyl-6-(benzyloxymethyl)morpholin-2-yl)methanol is used as a subject of research and development in both academia and the pharmaceutical industry. Its unique structure and potential applications make it an interesting compound to explore for the discovery of new chemical reactions and the development of novel therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 1093085-89-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,3,0,8 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1093085-89:
(9*1)+(8*0)+(7*9)+(6*3)+(5*0)+(4*8)+(3*5)+(2*8)+(1*9)=162
162 % 10 = 2
So 1093085-89-2 is a valid CAS Registry Number.

1093085-89-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name {(2R,6S)-4-Benzyl-6-[(benzyloxy)methyl]-2-morpholinyl}methanol

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:1093085-89-2 SDS

1093085-89-2Downstream Products

1093085-89-2Relevant academic research and scientific papers

NOVEL RENIN INHIBITOR

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Paragraph 0490; 0491; 0506; 0507, (2015/09/22)

The present invention provides a nitrogen-containing saturated heterocyclic compound of the formula [I] which is useful as a renin inhibitor. wherein R1 is a cycloalkyl group or an alkyl, R22 is an optionally substituted aryl and the like, R is a lower alkyl group, R3, R4, R5 and R6 are the same or different, and are a hydrogen atom, an optionally substituted carbamoyl, an optionally substituted alkyl, or alkoxycarbonyl, or a pharmaceutically acceptable salt thereof.

Morpholinyl acetamide derivatives and use thereof

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, (2008/06/13)

Morpholinyl acetamide derivatives are provided having the structure STR1 wherein R is hydrogen, lower alkyl, lower alkenyl or lower alkanoyl, R1 and R2 may be the same or different and are lower alkyl, lower alkenyl, phenyl-lower alk

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