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1-BOC-2-METHYLPIPECOLINIC ACID is a chemical compound with the molecular formula C11H19NO4, derived from pipecolic acid and featuring a BOC (tert-butoxycarbonyl) protecting group. 1-BOC-2-METHYLPIPECOLINIC ACID is recognized for its versatility in organic synthesis, serving as a building block for the preparation of pharmaceuticals and other organic compounds. Its BOC protecting group allows for mild deprotection conditions, enhancing its utility as an intermediate in chemical reactions. Additionally, 1-BOC-2-METHYLPIPECOLINIC ACID holds promise as a chiral auxiliary in asymmetric synthesis, contributing to the development of enantioselective processes.

746658-74-2

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746658-74-2 Usage

Uses

Used in Pharmaceutical Industry:
1-BOC-2-METHYLPIPECOLINIC ACID is used as a key intermediate in the synthesis of various pharmaceuticals due to its ability to be incorporated into complex molecular structures. The presence of the BOC protecting group facilitates the controlled formation of amide bonds, which are crucial in the construction of peptide-based drugs.
Used in Organic Synthesis:
1-BOC-2-METHYLPIPECOLINIC ACID is utilized as a versatile building block in organic synthesis for the preparation of a wide range of organic compounds. Its BOC protecting group can be selectively removed under mild conditions, enabling the synthesis of target molecules with high yields and purity.
Used in Asymmetric Synthesis:
1-BOC-2-METHYLPIPECOLINIC ACID is employed as a chiral auxiliary in asymmetric synthesis, aiding in the development of enantioselective processes. Its unique structural features enable the selective formation of desired enantiomers, which is critical in the production of biologically active compounds with specific pharmacological properties.
Used in Research and Development:
1-BOC-2-METHYLPIPECOLINIC ACID is used as a valuable tool in research and development for exploring new synthetic routes and methodologies. Its reactivity and selectivity in various chemical transformations provide insights into the underlying mechanisms and help in the design of novel synthetic strategies.

Check Digit Verification of cas no

The CAS Registry Mumber 746658-74-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,6,6,5 and 8 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 746658-74:
(8*7)+(7*4)+(6*6)+(5*6)+(4*5)+(3*8)+(2*7)+(1*4)=212
212 % 10 = 2
So 746658-74-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H21NO4/c1-11(2,3)17-10(16)13-8-6-5-7-12(13,4)9(14)15/h5-8H2,1-4H3,(H,14,15)

746658-74-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-1-[(2-methylpropan-2-yl)oxycarbonyl]piperidine-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 1-Boc-2-methyl-2-piperidinecarboxylic acid

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:746658-74-2 SDS

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