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(S)-1-BOC-3-AMINO-PYRROLIDINE HCL, with the molecular formula C9H17NO2, is the hydrochloride salt form of the (S)-enantiomer of 1-BOC-3-amino-pyrrolidine. This chemical compound serves as a chiral building block in organic synthesis, playing a crucial role in the preparation of pharmaceuticals, agrochemicals, and other fine chemicals. The BOC (tert-butoxycarbonyl) protecting group ensures the stability of the amino group, enabling selective reactivity manipulation during chemical reactions. Present as a white to off-white solid, it requires careful handling and storage under controlled conditions to prevent degradation. Safety guidelines must be adhered to, as it can cause skin and eye irritation.

874140-63-3

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874140-63-3 Usage

Uses

Used in Pharmaceutical Industry:
(S)-1-BOC-3-AMINO-PYRROLIDINE HCL is used as a chiral building block for the synthesis of various pharmaceuticals. Its unique (S)-enantiomer configuration and BOC protecting group allow for the creation of enantiomerically pure compounds, which are essential for the development of effective and safe medications.
Used in Agrochemical Industry:
In the agrochemical industry, (S)-1-BOC-3-AMINO-PYRROLIDINE HCL is utilized as a chiral intermediate for the synthesis of agrochemicals. Its ability to form enantiomerically pure compounds contributes to the development of targeted and environmentally friendly pesticides and other agricultural products.
Used in Fine Chemicals Industry:
(S)-1-BOC-3-AMINO-PYRROLIDINE HCL is employed as a key component in the synthesis of fine chemicals. Its versatility and the presence of the BOC protecting group make it suitable for the preparation of high-quality specialty chemicals used in various applications, such as fragrances, dyes, and other specialty products.

Check Digit Verification of cas no

The CAS Registry Mumber 874140-63-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,4,1,4 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 874140-63:
(8*8)+(7*7)+(6*4)+(5*1)+(4*4)+(3*0)+(2*6)+(1*3)=173
173 % 10 = 3
So 874140-63-3 is a valid CAS Registry Number.

874140-63-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl (3S)-3-aminopyrrolidine-1-carboxylate,hydrochloride

1.2 Other means of identification

Product number -
Other names (S)-1-Boc-3-Amino-pyrrolidine hydrochloride

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:874140-63-3 SDS

874140-63-3Downstream Products

874140-63-3Relevant academic research and scientific papers

THERAPEUTIC AGENT FOR CEREBRAL INFARCTION

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, (2012/08/08)

The invention provides a therapeutic drug for ischemic stroke. The therapeutic drug has the formula (I) wherein each symbol is as defined herein, or a pharmacologically acceptable salt thereof, or a solvate thereof, as an active ingredient.

METHOD FOR PRODUCTION OF OPTICALLY ACTIVE 3-AMINO-NITROGENATED COMPOUND

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Page/Page column 22, (2009/05/29)

Aiming at production of an optically active 3-amino nitrogen-containing compound which is useful as an intermediate in synthesis of medicines and pesticides, in particular, an optically active 1-protected-3-aminopyrrolidine derivative, from an inexpensive and readily available raw material by a process which is efficient and can be practiced industrially, an optically active 3-amino nitrogen-containing compound is produced by performing a reaction of an optically active 3-substituted nitrogen-containing compound with ammonia, methylamine, ethylamine or dimethylamine in the presence of water. In addition, a 1-protected-3-aminopyrrolidine derivative is produced by performing a reaction of an optically active 1-protected-3-(sulfonyloxy)pyrrolidine derivative with ammonia, methylamine, ethylamine, or dimethylamine in the presence of methanol, ethanol, n-propanol, or isopropanol under a pressure of less than 30 barr.

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