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40248-34-8

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  • 2,2,2-trifluoro-n-(6-hydroxyhexyl)acetamide CAS NO.40248-34-8 CAS NO.40248-34-8

    Cas No: 40248-34-8

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  • Acetamide,2,2,2-trifluoro-N-(6-hydroxyhexyl)-

    Cas No: 40248-34-8

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40248-34-8 Usage

Chemical Properties

Pale Yellow Solid

Uses

N-(Trifluoroacetyl)hexanolamine can be used as biosensors with pH-independent redox moieties.

Check Digit Verification of cas no

The CAS Registry Mumber 40248-34-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,2,4 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 40248-34:
(7*4)+(6*0)+(5*2)+(4*4)+(3*8)+(2*3)+(1*4)=88
88 % 10 = 8
So 40248-34-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H14F3NO2/c9-8(10,11)7(14)12-5-3-1-2-4-6-13/h13H,1-6H2,(H,12,14)

40248-34-8 Well-known Company Product Price

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  • Aldrich

  • (91679)  N-(6-Hydroxyhexyl)trifluoroacetamide  ≥98.0% (GC)

  • 40248-34-8

  • 91679-1G

  • 783.90CNY

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40248-34-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,2-trifluoro-N-(6-hydroxyhexyl)acetamide

1.2 Other means of identification

Product number -
Other names N-(Trifluoroacetyl)hexanolamine

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:40248-34-8 SDS

40248-34-8Relevant articles and documents

OLIGONUCLEOTIDE COMPOSITIONS AND METHODS THEREOF

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Paragraph 00735-00736, (2021/11/26)

The present disclosure provides modified oligonucleotides and compositions and methods thereof. In some embodiments, provided technologies comprise modified sugars and/or modified internucleotidic linkages. In some embodiments, the present disclosure provides technologies for preparing modified oligonucleotides. In some embodiments, the present disclosure provides chirally controlled oligonucleotide compositions and methods for their preparation and uses.

Rapid Synthesis of Bicyclic N-Heterocyclic Cores from N-Terminal α,β-Unsaturated Diazoketones

Santiago, Jo?o Victor,Burtoloso, Antonio C. B.

, p. 2822 - 2830 (2018/06/04)

A method for the synthesis of bicyclic N-heterocyclic cores from N-terminal α,β-unsaturated diazoketones has been developed. The transformation involves three sequential steps that include N-deprotection, an intramolecular aza-Michael, and a photochemical Wolff rearrangement as a one-pot protocol. By using this strategy, a series of substituted bicyclic N-heterocycles, particularly, indolizidines and pyrrolizidines, were synthesize in good yields.

NOVEL LIVER-TARGETING AGENTS AND THEIR SYNTHESIS

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Page/Page column 1; 2, (2011/04/19)

This invention provides novel liver targeting agents and their synthetic methods. A liver targeting agent, with a lysine based nitrilo triacetic acid structure as backbone which acquires multivalency with saccharide groups, to bind with a galactosamine chain or lactose chain is disclosed. In particular, only one amino acid L-lysine is involved to provide trivalency. All carboxyl groups in Nε-benzyloxycarbonyl-Nα-dicarboxymethyl-L-lysine can be conjugated with three glycosides of ahGalNAc or ahLac in one step. This invention also provides a hexa-lactoside. In particular, the TFA-AHA-Asp was used to conjugate 2 moles of NTA(ahLac)3. This invention also provides a method for adding a spacer between NTA and DTPA. The extended hepatocyte-specific glyco-ligand has higher 111In-radiolabelling yield than those non-extended.

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