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284049-22-5

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284049-22-5 Usage

Description

Carbamic acid, (2-isocyanatoethyl)-, 1,1-dimethylethyl ester (9CI), also known as tert-Butyl N-(2-Isocyanatoethyl)carbamate, is a chemical compound with potential applications in various fields, particularly in the medical and pharmaceutical industries. It is characterized by its isocyanate functional group, which allows for further chemical reactions and modifications.

Uses

Used in Pharmaceutical Industry:
Carbamic acid, (2-isocyanatoethyl)-, 1,1-dimethylethyl ester (9CI) is used as an active pharmaceutical ingredient for the treatment of various medical conditions, such as cancer, fatty liver, and inflammation. Its isocyanate group enables it to interact with biological targets and modulate their activity, making it a promising candidate for drug development.
Used in Cancer Treatment:
In the field of oncology, Carbamic acid, (2-isocyanatoethyl)-, 1,1-dimethylethyl ester (9CI) is used as a chemotherapeutic agent for the treatment of various types of cancer. Its isocyanate group can potentially react with cellular components, leading to the disruption of cancer cell growth and proliferation.
Used in Treatment of Fatty Liver:
Carbamic acid, (2-isocyanatoethyl)-, 1,1-dimethylethyl ester (9CI) is also used as a therapeutic agent for the treatment of fatty liver disease. Its ability to modulate cellular processes may help in reducing the accumulation of fat in the liver and improving liver function.
Used in Anti-Inflammatory Applications:
In the context of inflammation, Carbamic acid, (2-isocyanatoethyl)-, 1,1-dimethylethyl ester (9CI) is used as an anti-inflammatory agent. Its potential to interact with cellular targets and modulate inflammatory pathways may help in reducing inflammation and alleviating symptoms associated with various inflammatory conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 284049-22-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,4,0,4 and 9 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 284049-22:
(8*2)+(7*8)+(6*4)+(5*0)+(4*4)+(3*9)+(2*2)+(1*2)=145
145 % 10 = 5
So 284049-22-5 is a valid CAS Registry Number.

284049-22-5SDS

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 N-(2-isocyanatoethyl)carbamate

1.2 Other means of identification

Product number -
Other names Carbamic acid,N-(2-isocyanatoethyl)-,1,1-dimethyl ethyl ester

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:284049-22-5 SDS

284049-22-5Relevant articles and documents

A CONJUGATE OF A CYTOTOXIC AGENT TO A CELL BINDING MOLECULE WITH BRANCHED LINKERS

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Page/Page column 249, (2021/01/23)

Provided is a conjugation of cytotoxic drug to a cell-binding molecule with a side-chain linker. It provides side-chain linkage methods of making a conjugate of a cytotoxic molecule to a cell-binding ligand, as well as methods of using the conjugate in targeted treatment of cancer, infection and immunological disorders.

A nonpeptidic reverse-turn scaffold stabilized by urea-based dual intramolecular hydrogen bonding

Medda, Amiya K.,Park, Chul Min,Jeon, Aram,Kim, Hyunwoo,Sohn, Jeong-Hun,Lee, Hee-Seung

supporting information; experimental part, p. 3486 - 3489 (2011/09/12)

A novel nonpeptidic reverse-turn scaffold containing urea fragments that are connected by a conformationally constrained d-prolyl-cis-1,2- diaminocyclohexane (d-Pro-DACH) linker is reported. The scaffold adopts a well-defined reverse-turn conformation tha

Effective preparation of O-succinimidyl-2(tert- butoxycarbonylamino)ethylcarbamate derivatives from β-amino acids. Application to the synthesis of urea-containing pseudopeptides and oligoureas

Guichard, Gilles,Semetey, Vincent,Didierjean, Claude,Aubry, Andre,Briand, Jean-Paul,Rodriguez, Marc

, p. 8702 - 8705 (2007/10/03)

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