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(2S,3R)-benzyl 3-(tert-butoxycarbonyl)-2-methylpiperidine-1-carboxylate is a heterocyclic organic compound derived from piperidine, featuring a benzyl group, a tert-butoxycarbonyl group, and a methylpiperidine carboxylate group. The (2S,3R) stereochemistry denotes the specific spatial arrangement of its atoms, which may contribute to its potential applications in medicinal chemistry and as a precursor for synthesizing other organic compounds. (2S,3R)-benzyl 3-(tert-butoxycarbonyl)-2-methylpiperidine-1-carboxylate may also possess biological activity, making it a candidate for drug development.

1044563-67-8

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  • (2S,3R)-1-BENZYL 3-TERT-BUTYL 2-METHYLPIPERIDINE-1,3-DICARBOXYLATE

    Cas No: 1044563-67-8

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1044563-67-8 Usage

Uses

Used in Pharmaceutical Synthesis:
(2S,3R)-benzyl 3-(tert-butoxycarbonyl)-2-methylpiperidine-1-carboxylate is used as a building block in the synthesis of various pharmaceuticals due to its unique structural features and potential for chemical modification.
Used in Medicinal Chemistry:
(2S,3R)-benzyl 3-(tert-butoxycarbonyl)-2-methylpiperidine-1-carboxylate is used as a compound in medicinal chemistry for its potential to be developed into a drug candidate, given its specific stereochemistry and the presence of functional groups that can be exploited for biological activity.
Used in Drug Development:
In the pharmaceutical industry, (2S,3R)-benzyl 3-(tert-butoxycarbonyl)-2-methylpiperidine-1-carboxylate is used as a starting material for drug development, leveraging its heterocyclic nature and the possibility of its biological activity for the creation of new therapeutic agents.
Used in Organic Synthesis:
(2S,3R)-benzyl 3-(tert-butoxycarbonyl)-2-methylpiperidine-1-carboxylate is used as a versatile intermediate in organic synthesis, allowing for the construction of complex organic molecules for various applications, including but not limited to, the development of new materials and chemical compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 1044563-67-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,4,5,6 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1044563-67:
(9*1)+(8*0)+(7*4)+(6*4)+(5*5)+(4*6)+(3*3)+(2*6)+(1*7)=138
138 % 10 = 8
So 1044563-67-8 is a valid CAS Registry Number.

1044563-67-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,3R)-1-Benzyl 3-tert-butyl 2-methylpiperidine-1,3-dicarboxylate

1.2 Other means of identification

Product number -
Other names 1-O-benzyl 3-O-tert-butyl (2S,3R)-2-methylpiperidine-1,3-dicarboxylate

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:1044563-67-8 SDS

1044563-67-8Downstream Products

1044563-67-8Relevant articles and documents

INHIBITORS OF BRUTON'S TYROSINE KINASE

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, (2015/06/17)

Disclosed herein are reversible and irreversible inhibitors of Bruton's tyrosine kinase (Btk). Also disclosed are pharmaceutical compositions that include the compounds. Methods of using the Btk inhibitors are described, alone or in combination with other

AMIDE DERIVATIVE

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Page/Page column 169, (2009/12/05)

The present invention relates to a compound of the formula (I) being useful as a renin inhibitor, or a pharmaceutically acceptable salt thereof. wherein R1a is a hydrogen atom, an optionally substituted C1-6 alkyl, etc.; R1b is an optionally substituted C1-6 alkoxy, etc.; R1c is a hydrogen atom, an optionally substituted C1-6 alkoxy, etc.; R2 is a hydrogen atom, an optionally substituted C1-6 alkyl, etc.; R3a, R3b, R3c and R3d are independently the same or different, and each is a group of the formula: -A-B (in which A is a single bond, -(CH2)sO-, - (CH2)sN(R4)CO-, etc., B is a hydrogen atom, an optionally substituted C1-6 alkyl, etc.), etc.; R4 is a hydrogen atom, an optionally substituted C1-6 alkyl, etc.; s is 0, etc.; and n is 1, etc.

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