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(S)-3-(TERT-BUTOXYCARBONYL)-2,2-DIMETHYLOXAZOLIDINE-4-CARBOXYLIC ACID is a chemical compound that belongs to the category of organic compounds known as oxazolidines. It is characterized by an oxazolidine ring which is a five-membered cyclic compound containing two carbon atoms, one nitrogen atom, and one oxygen atom. The term "tert-butoxycarbonyl" in its name signifies the presence of a protective group used primarily in peptide synthesis. Its primary role is to prevent unwanted peptide bond formation by temporarily blocking the reactive amine group during synthesis. Combined, all these characteristics suggest this chemical plays a role in pharmaceutical synthesis or other chemical synthetic processes requiring protective groups.

139009-66-8

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  • (S)-3-(TERT-BUTOXYCARBONYL)-2,2-DIMETHYLOXAZOLIDINE-4-CARBOXYLIC ACID

    Cas No: 139009-66-8

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139009-66-8 Usage

Uses

Used in Pharmaceutical Synthesis:
(S)-3-(TERT-BUTOXYCARBONYL)-2,2-DIMETHYLOXAZOLIDINE-4-CARBOXYLIC ACID is used as a protective group in peptide synthesis for preventing unwanted peptide bond formation. This is particularly important in the development of new drugs and therapeutic agents, where precise control over the synthesis process is crucial for achieving the desired molecular structure and biological activity.
Used in Chemical Synthesis Processes:
In chemical synthesis processes that require the use of protective groups, (S)-3-(TERT-BUTOXYCARBONYL)-2,2-DIMETHYLOXAZOLIDINE-4-CARBOXYLIC ACID is used as a temporary blocking agent to protect reactive amine groups. This allows for more controlled and selective reactions, leading to the production of complex molecules with specific properties and functions.

Check Digit Verification of cas no

The CAS Registry Mumber 139009-66-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,0,0 and 9 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 139009-66:
(8*1)+(7*3)+(6*9)+(5*0)+(4*0)+(3*9)+(2*6)+(1*6)=128
128 % 10 = 8
So 139009-66-8 is a valid CAS Registry Number.

139009-66-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-N-Boc-2,2-dimethyloxazolidine-4-carboxylic Acid

1.2 Other means of identification

Product number -
Other names (S)-3-(tert-Butoxycarbonyl)-2,2-dimethyloxazolidine-4-carboxylic 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:139009-66-8 SDS

139009-66-8Relevant articles and documents

Efficient construction of a doubly functionalized trisoxazole derivative relevant to the synthesis of the novel telomerase inhibitor telomestatin and its analogues

Chattopadhyay, Shital K.,Biswas, Suman,Pal, Benoy K.

, p. 1289 - 1294 (2006)

An efficient construction of a suitably functionalized trisoxazole derivative related to telomestatin was developed from L-serine, which involved three sequential oxazoline cyclization-oxidation steps in an overall yield of 11% in a linear sequence of twelve steps. Georg Thieme Verlag Stuttgart.

Capturing Intermediates in the Reaction Catalyzed by NosN, a Class C Radical S-Adenosylmethionine Methylase Involved in the Biosynthesis of the Nosiheptide Side-Ring System

Wang, Bo,Lamattina, Joseph W.,Marshall, Savannah L.,Booker, Squire J.

supporting information, (2019/04/17)

Nosiheptide is a ribosomally synthesized and post-translationally modified thiopeptide natural product that possesses antibacterial, anticancer, and immunosuppressive properties. It contains a bicyclic structure composed of a large macrocycle and a unique

Capturing Intermediates in the Reaction Catalyzed by NosN, a Class C Radical S-Adenosylmethionine Methylase Involved in the Biosynthesis of the Nosiheptide Side-Ring System

Wang, Bo,Lamattina, Joseph W.,Marshall, Savannah L.,Booker, Squire J.

supporting information, p. 5788 - 5797 (2019/04/17)

Nosiheptide is a ribosomally synthesized and post-translationally modified thiopeptide natural product that possesses antibacterial, anticancer, and immunosuppressive properties. It contains a bicyclic structure composed of a large macrocycle and a unique

[4-(1, 3, 3-TRIMETHYL-2-OXO-3, 4-DIHYDRO-1H-QUINOXALIN-7-YL) PHENOXY]ETHYLOXY COMPOUND OR SALT THEREOF

-

Paragraph 0123; 0125, (2018/07/29)

The present invention relates to a novel [4-(1,3,3-trimethyl-2-oxo-3,4-dihydro-1H-quinoxalin-7-yl)phenoxy]ethyloxy compound or a salt thereof. The compound or a salt thereof of the present invention has a glucocorticoid receptor agonist activity, and is u

Total synthesis of the azolemycins

Anderson, Zoe J.,Fox, David J.

, p. 1450 - 1454 (2016/02/03)

The first total syntheses of newly isolated polyazole natural products azolemycins A-D, along with the synthesis of the tetra-oxazole non-natural analogue, are described.

BROMODOMAIN-INHIBITING COMPOUNDS AND PHARMACEUTICAL COMPOSITION COMPRISING SAME FOR PREVENTING OR TREATING A CANCER

-

Page/Page column 23; 25; 26, (2015/11/27)

Provided is a novel compound having bromodomain and extra terminal domain (BET) protein inhibiting activities, and a pharmaceutical composition comprising the same which can be useful for prevention or treatment of precancerous transformation or cancer.

Hepatitis C Virus Inhibitors

-

Paragraph 1778-1779, (2015/02/25)

The present disclosure is generally directed to antiviral compounds, and more specifically directed to combinations of compounds which can inhibit the function of the NS5A protein encoded by Hepatitis C virus (HCV), compositions comprising such combinations, and methods for inhibiting the function of the NS5A protein.

COMBINATIONS OF HEPATITIS C VIRUS INHIBITORS

-

Page/Page column 593; 594, (2015/02/02)

The present disclosure is generally directed to antiviral compounds, and more specifically directed to combinations of compounds which can inhibit the function of the NS5A protein encoded by Hepatitis C virus (HCV), compositions comprising such combinations, and methods for inhibiting the function of the NS5A protein.

Total synthesis and biological activity of natural product Urukthapelstatin A

Lin, Chun-Chieh,Tantisantisom, Worawan,McAlpine, Shelli R.

supporting information, p. 3574 - 3577 (2013/08/23)

Herein we report the first total synthesis of the natural product Urkuthaplestatin A (Ustat A) utilizing a convergent synthetic strategy. The characterization and biological activity match those of the previously published natural product. Interestingly,

A convenient procedure for the preparation of Garner's aldehyde

Trajkovic, Milos,Ferjancic, Zorana,Saicic, Radomir N.

, p. 602 - 604 (2012/08/13)

The palladium/silane reduction of a serine thioester derivative allows for the preparation of enantiomerically pure Garner's aldehyde from serine, in gram quantities within 24 h.

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