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139115-92-7

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139115-92-7 Usage

Description

N-Boc-PEG3-alcohol is a PEG linker containing a hydroxyl group and Boc-protected amino group. The hydrophilic PEG spacer increases solubility in aqueous media. The hydroxyl group enables further derivatization or replacement with other reactive functional groups. The Boc group can be deprotected under mild acidic conditions to form the free amine.

Chemical Properties

Colourless Oil

Uses

A cross-linking reagent

Check Digit Verification of cas no

The CAS Registry Mumber 139115-92-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,1,1 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 139115-92:
(8*1)+(7*3)+(6*9)+(5*1)+(4*1)+(3*5)+(2*9)+(1*2)=127
127 % 10 = 7
So 139115-92-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H23NO5/c1-11(2,3)17-10(14)12-4-6-15-8-9-16-7-5-13/h13H,4-9H2,1-3H3,(H,12,14)

139115-92-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-(2-t-Boc-aminoethoxy]ethoxy]ethanol

1.2 Other means of identification

Product number -
Other names tert-Butyl (2-(2-(2-hydroxyethoxy)ethoxy)ethyl)carbamate

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:139115-92-7 SDS

139115-92-7Downstream Products

139115-92-7Relevant articles and documents

Design, synthesis, and biological evaluation of biotin-labeled (-)-ternatin, a potent fat-accumulation inhibitor against 3T3-L1 adipocytes

Shimokawa, Kenichiro,Yamada, Kaoru,Ohno, Osamu,Oba, Yuichi,Uemura, Daisuke

, p. 92 - 95 (2009)

The design, synthesis, and biological activity of biotin-labeled (-)-ternatin are reported. Chemical modification, that is, biotinylation, was conducted using Click chemistry at the 6-position (NMe-d-ProGly moiety), which was a plausible location selected

EXPANSION MICROSCOPY COMPATIBLE ANCHORABLE HandE STAINING FOR HISTOPATHOLOGY

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, (2022/03/18)

The present invention employs the technique for expansion microscopy (E×M) utilizing anchorable derivatives of hematoxylin and eosin (HandE) stained tissue specimens within tissue samples, in order to achieve high resolution detection of biomolecules with precise morphological features of cells and nuclei, which in turn, allows for effective for accurate early stage disease diagnosis including various cancers. Staining with HandE employs anchorable derivatives that can be cross-linked into the E×M hydrogel matrix.

Small molecule compound based on EZH2 protein degradation, and application thereof

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Paragraph 0103-0106, (2021/08/07)

The invention discloses a series of small molecule compounds capable of selectively degrading EZH2 protein, and application thereof. The compounds can be prepared into proper pharmaceutical dosage forms for EZH2-mediated related tumor treatment.

Heterocyclic compound and application thereof

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Paragraph 1323-1327, (2021/08/07)

The invention discloses a heterocyclic compound and application thereof. The invention provides a heterocyclic compound as shown in a formula I, or pharmaceutically acceptable salt thereof. The heterocyclic compound can be used for degrading ALK, c-Met and ROS proteins.

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