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(2S)-2-[3-(TERT-BUTOXYCARBONYL)-2,2-DIMETHYLPROPANOYL]OXY-4-METHYLPENTANOIC ACID is a chiral chemical compound characterized by the presence of a carboxylic acid, ester, and alkyl groups. It features a stereocenter at the second carbon and has a molecular formula of C18H32O6. (2S)-2-[3-(TERT-BUTOXYCARBONYL)-2,2-DIMETHYLPROPANOYL]OXY-4-METHYLPENTANOIC ACID is recognized for its diverse reactivity and potential to generate new molecules with specific biological activities, making it a valuable asset in organic synthesis and pharmaceutical drug development.

186193-10-2

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186193-10-2 Usage

Uses

Used in Organic Synthesis:
(2S)-2-[3-(TERT-BUTOXYCARBONYL)-2,2-DIMETHYLPROPANOYL]OXY-4-METHYLPENTANOIC ACID serves as a versatile building block in organic synthesis, where its functional groups can be manipulated to create a variety of new molecules with tailored properties.
Used in Pharmaceutical Drug Development:
In the pharmaceutical industry, (2S)-2-[3-(TERT-BUTOXYCARBONYL)-2,2-DIMETHYLPROPANOYL]OXY-4-METHYLPENTANOIC ACID is utilized for the development of drugs with specific biological activities. Its chiral nature and diverse reactivity contribute to the design of novel therapeutic agents.
Used in Chemical Research:
(2S)-2-[3-(TERT-BUTOXYCARBONYL)-2,2-DIMETHYLPROPANOYL]OXY-4-METHYLPENTANOIC ACID is also employed as a valuable tool in chemical research. Its tert-butoxycarbonyl protecting group allows for selective removal, revealing reactive functional groups that can be further manipulated for synthetic purposes, thus aiding in the advancement of chemical knowledge and techniques.

Check Digit Verification of cas no

The CAS Registry Mumber 186193-10-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,6,1,9 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 186193-10:
(8*1)+(7*8)+(6*6)+(5*1)+(4*9)+(3*3)+(2*1)+(1*0)=152
152 % 10 = 2
So 186193-10-2 is a valid CAS Registry Number.

186193-10-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-<3-<<(1-dimethylethoxy)carbonyl>amino>-2,2-dimethyl-1-oxopropoxy>-4-methylpentanoic acid

1.2 Other means of identification

Product number -
Other names (S)-2-(3-tert-Butoxycarbonylamino-2,2-dimethyl-propionyloxy)-4-methyl-pentanoic 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:186193-10-2 SDS

186193-10-2Relevant academic research and scientific papers

BIOCATALYTIC SYNTHESIS OF CRYPTOPHYCIN ANTICANCER AGENTS

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Paragraph 0021; 0131; 0132, (2021/04/02)

The disclosure provides cryptophycin intermediates, cryptophycin analogs, and cryptophycin chimeric molecules useful in treating cancer, as well as methods of producing these compounds and methods of treating cancer.

A versatile chemoenzymatic synthesis for the discovery of potent cryptophycin analogs

Brody, Scott I.,Khatri, Yogan,Pietraszkiewicz, Halina,Schmidt, Jennifer J.,Sherman, David H.,Valeriote, Frederick A.,Zhu, Catherine

, p. 524 - 532 (2020/03/11)

The cryptophycins are a family of macrocyclic depsipeptide natural products that display exceptionally potent antiproliferative activity against drug-resistant cancers. Unique challenges facing the synthesis and derivatization of this complex group of molecules motivated us to investigate a chemoenzymatic synthesis designed to access new analogs for biological evaluation. The cryptophycin thioesterase (CrpTE) and the cryptophycin epoxidase (CrpE) are a versatile set of enzymes that catalyze macrocyclization and epoxidation of over 20 natural cryptophycin metabolites. Thus, we envisioned a drug development strategy involving their use as standalone biocatalysts for production of unnatural derivatives. Herein, we developed a scalable synthesis of 12 new unit A-B-C-D linear chain elongation intermediates containing heterocyclic aromatic groups as alternatives to the native unit A benzyl group. N-Acetyl cysteamine activated forms of each intermediate were assessed for conversion to macrocyclic products using wild type CrpTE, which demonstrated the exceptional flexibility of this enzyme. Semipreparative scale reactions were conducted for isolation and structural characterization of new cryptophycins. Each was then evaluated as a substrate for CrpE P450 and its ability to generate the epoxidized products from these substrates that possess altered electronics at the unit A styrenyl double bond position. Finally, biological evaluation of the new cryptophycins revealed a des-β-epoxy analog with low picomolar potency, previously limited to cryptophycins bearing epoxide functionality.

Enantioselective Synthesis of (+)-Cryptophycin 52 (LY355703), a Potent Antimitotic Antitumor Agent

Ghosh, Arun K.,Swanson, Lisa

, p. 9823 - 9826 (2007/10/03)

A highly enantioselective and convergent synthesis of cryptophycin 52 (2), an exceedingly potent cytotoxic agent, is described. Cryptophycin 52, a synthetic variant of the cryptophycin family, is currently undergoing clinical trials. The synthesis is conv

Cryptophycins from synthesis

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, (2008/06/13)

A cryptophycin compound is provided having the structure: Further provided are methods of producing cryptophycins by total synthesis and methods of using cryptophycins in pharmaceuticals. It is a further object of this invention to use cryptophycins to inhibit the proliferation of mammalian cells. Moreover, methods of using cryptophycins to treat neoplasia is also provided.

A novel approach for total synthesis of cryptophycins via asymmetric crotylboration protocol

Dhokte, Ulhas P.,Khau, Vien V.,Hutchison, Darrell R.,Martinelli, Michael J.

, p. 8771 - 8774 (2007/10/03)

Acyclic and a highly efficient stereoselective C-C bond formation of aldehyde 3 with the crotylboron reagent 4, derived from (-)-α-pinene, provided a homoallylic alcohol 6 in ≥99% enantio-(ee) and diastereomeric excess (de). The alcohol 6 was linearly con

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