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169870-82-0

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169870-82-0 Usage

General Description

N-BOC-T-Butylglycine is a type of synthetic compound regularly used in pharmaceuticals and organic synthesis for drug development. Additionally, it plays a key role in the preparation of enzyme inhibitors. This chemical, also recognized as N-Theoretical-Boc-T-Butylglycine, can be used for synthesizing peptidomimetics and as a building block for beta-turn mimetics. It often exists as a white crystalline powder, and it must be handled with care due to its potential hazards such as causing skin and eye irritation and specific target organ toxicity. As a laboratory reagent, this protected amino acid is also used in peptide and other organic syntheses.

Check Digit Verification of cas no

The CAS Registry Mumber 169870-82-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,8,7 and 0 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 169870-82:
(8*1)+(7*6)+(6*9)+(5*8)+(4*7)+(3*0)+(2*8)+(1*2)=190
190 % 10 = 0
So 169870-82-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H21NO4/c1-10(2,3)12(7-8(13)14)9(15)16-11(4,5)6/h7H2,1-6H3,(H,13,14)

169870-82-0SDS

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 N-BOC-T-BUTYLGLYCINE

1.2 Other means of identification

Product number -
Other names N-Boc-tert-leucine

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:169870-82-0 SDS

169870-82-0Relevant articles and documents

Preparation method of racemic D/L-tert-leucine

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Paragraph 0044-0046, (2020/06/20)

The invention discloses a preparation method of racemic D/L-tert-leucine, and belongs to the technical field of organic synthesis. Tert-butylpyruvic acid is used as a raw material, and racemic D/L-tert-leucine is obtained through a two-step reaction, wherein in the first step, a Schiff base is generated through a condensation reaction with NH2-P and in the second step, the Schiff base is reduced,deprotection is carried out by using an acid, and the base is adjusted to an isoelectric point to obtain the racemic D/L-tert-leucine. The method is simple and convenient to operate and high in reaction yield, and the purity of the obtained raceme can reach 99% or above.

PROCESS FOR PRODUCTION OF N-ALKOXYCARBONYL-tert-LEUCINES

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Page/Page column 14, (2012/03/26)

A high quality N-alcoxycarbonyl-tert leucine can be efficiently and stably produced with an easy procedure by reacting tert-leucine with an N-alcoxycarbonylating agent in the presence of water, wherein the use amount of the N-alcoxycarbonylating agent is not less than 0.90 times by mole and not more than 1.00 times by mole relative to the tert-leucine, with maintaining the pH of the reaction mixture in the range of not less than 9 and not more than 13 using a basic agent. In addition, an N-alcoxycarbonyl-tert-leucine can be efficiently extracted from the basic aqueous solution thereof under a mild condition using a water-immiscible solvent by mixing a hydroxide. Furthermore, the two crystal forms of N-butoxycarbonyl-tert-leucine can be controlled by adjusting the water amount in crystallization step, and the compound can be stably produced in an industrial production.

Potassium channel openers

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, (2008/06/13)

Compounds of formula I: are useful in treating diseases prevented by or ameliorated with potassium channel openers. Also disclosed are potassium channel opening compositions and a method of opening potassium channels in a mammal.

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