Welcome to LookChem.com Sign In|Join Free
  • or
Tert-butyl (1S,2R)-2-hydroxycyclopentylcarbaMate is a chiral chemical compound with the molecular formula C11H21NO3. It is an ester derivative of tert-butyl carbamate, featuring a cyclopentylcarbaMate moiety with a hydroxy group attached to the second carbon atom. tert-butyl (1S,2R)-2-hydroxycyclopentylcarbaMate is characterized by its stereochemistry, with stereocenters at the first and second carbon atoms. The tert-butyl group imparts steric hindrance and stability, making it a valuable building block in the synthesis of biologically active compounds.

913631-66-0

Post Buying Request

913631-66-0 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

913631-66-0 Usage

Uses

Used in Organic Synthesis:
Tert-butyl (1S,2R)-2-hydroxycyclopentylcarbaMate is utilized as a reagent in organic synthesis for the preparation of various biologically active compounds. Its unique structure and stereochemistry make it a versatile component in the creation of complex organic molecules.
Used in Pharmaceutical Research:
In the pharmaceutical industry, tert-butyl (1S,2R)-2-hydroxycyclopentylcarbaMate serves as a key intermediate in the development of new drugs. Its properties, including the hydroxy group and the tert-butyl group, contribute to its potential as a precursor for medicinal compounds with therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 913631-66-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,3,6,3 and 1 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 913631-66:
(8*9)+(7*1)+(6*3)+(5*6)+(4*3)+(3*1)+(2*6)+(1*6)=160
160 % 10 = 0
So 913631-66-0 is a valid CAS Registry Number.

913631-66-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (1R,2S)-2-(BOC-amino)cyclopentanol

1.2 Other means of identification

Product number -
Other names -

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:913631-66-0 SDS

913631-66-0Downstream Products

913631-66-0Relevant academic research and scientific papers

PIPERIDINE COMPOUNDS AS MENIN INHIBITORS

-

Paragraph 000315-000316; 000524-000525, (2021/04/10)

The present disclosure provides compounds represented by Formula (la): and the pharmaceutically acceptable salts thereof, wherein R1a, R1b, R1c, R2, R3, L, M and G are as defined as set forth in the specification. The present disclosure also provides compounds of Formula la for use to treat a condition or disorder responsive to menin inhibition such as cancer.

MENIN INHIBITORS AND METHODS OF USE FOR TREATING CANCER

-

Paragraph 00551-00553, (2021/10/15)

The present disclosure provides compounds represented by Formula (I), or a pharmaceutically acceptable salt thereof, wherein Ra, Rb, Rc, Rd, V, Q, T, n, p, q, r and s are as defined as set forth in the specification. The present disclosure also provides compounds of Formula (I) for use to treat cancer or any other disease, condition, or disorder that is responsive to inhibition of menin.

SMALL MOLECULE MENIN INHIBITORS

-

Paragraph 0310, (2020/05/15)

The present disclosure provides compounds represented by Formula I: and the pharmaceutically acceptable salts and solvates thereof, wherein R1a, R1b, R1c, E, G, and Q are as defined as set forth in the specification. The present disclosure also provides compounds of Formula I for use to treat cancer or any other disease, condition, or disorder that is responsive to inhibition of menin.

INHIBITORS OF CYCLIN-DEPENDENT KINASE 7 (CDK7)

-

Paragraph 252, (2019/08/08)

The present invention provides, inter alia, compounds having the structures of formulas described herein; pharmaceutically acceptable salts, solvates, hydrates, tautomers, and isotopic forms thereof; and compositions (e.g., pharmaceutical compositions and kits) containing one or more of the foregoing. Also provided are methods of administering and uses involving the compounds and/or pharmaceutical compositions for treating or preventing disease. The disease can be a proliferative disease, such as a cancer (e.g., a blood cancer (e.g., a leukemia or lymphoma), a brain cancer, a breast cancer, melanoma, multiple myeloma, or an ovarian cancer) a benign neoplasm, pathologic angiogenesis, or a fibrotic disease. While no aspect of the invention is limited by the biological events that may transpire, administering a compound or other composition described herein may selectively inhibit the aberrant expression or activity of cyclin-dependent kinase 7 (CDK7) and, thereby, induce cellular apoptosis and/or inhibit the transcription of disease-related genes in the patient (or in a biological sample).

PIPERIDINES AS COVALENT MENIN INHIBITORS

-

Paragraph 0264, (2018/10/25)

The present disclosure provides compounds represented by Formula (I): and the pharmaceutically acceptable salts and solvates thereof, wherein A, R1a, R1b, R1c, R1d, R2, R3, R8a, R8b, R10, X, Z2, m, and n are as defined as set forth in the specification. The present disclosure also provides compounds of Formula (I) for use to treat a condition or disorder responsive to menin inhibition such as cancer.

BICYCLIC HETEROCYCLES AS FGFR4 INHIBITORS

-

Paragraph 0372, (2016/05/19)

The present invention relates to bicyclic heterocycles, and pharmaceutical compositions of the same, that are inhibitors of the FGFR4 enzyme and are useful in the treatment of FGFR4-associated diseases such as cancer.

Kinetic resolution of amino alcohol derivatives with a chiral nucleophilic catalyst: Access to enantiopure cyclic cis-amino alcohols

Kawabata,Yamamoto,Momose,Yoshida,Nagaoka,Fuji

, p. 2700 - 2701 (2007/10/03)

Acylative kinetic resolution of racemic cyclic cis-amino alcohol derivatives with a chiral nucleophilic catalyst proceeds enantioselectively (s = 10-21) at ambient temperature to give enantiopure recovered materials, and the % conversion of the acylation can be readily controlled by the amount of acid anhydride.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 913631-66-0