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284049-22-5

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284049-22-5 Usage

Uses

tert-Butyl N-(2-Isocyanatoethyl)carbamate, Technical Grade can be used to treat cancer, fatty liver, or inflammation.

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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