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[3,4,5-tris(phenylmethoxy)-6-(phenylmethoxymethyl)oxan-2-yl] 4-nitrobenzoate is a complex organic chemical compound characterized by the presence of phenylmethoxy groups, an oxan ring, and a nitrobenzoate group. Its structural complexity and the variety of functional groups it contains suggest potential for diverse chemical reactivity and applications.

54423-54-0

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54423-54-0 Usage

Uses

Given the provided materials, specific uses for [3,4,5-tris(phenylmethoxy)-6-(phenylmethoxymethyl)oxan-2-yl] 4-nitrobenzoate are not explicitly mentioned. However, based on the functional groups present, we can infer potential applications in various fields:
Used in Pharmaceutical Industry:
[3,4,5-tris(phenylmethoxy)-6-(phenylmethoxymethyl)oxan-2-yl] 4-nitrobenzoate could be used as a pharmaceutical intermediate for the synthesis of drugs targeting specific biological pathways due to its complex structure and functional groups.
Used in Chemical Research:
In the field of chemical research, [3,4,5-tris(phenylmethoxy)-6-(phenylmethoxymethyl)oxan-2-yl] 4-nitrobenzoate could serve as a subject for studying the reactivity of phenylmethoxy and nitrobenzoate groups, as well as the properties of the oxan ring.
Used in Material Science:
[3,4,5-tris(phenylmethoxy)-6-(phenylmethoxymethyl)oxan-2-yl] 4-nitrobenzoate might be utilized in the development of new materials, such as polymers or coatings, where its unique structure could impart specific properties.

Check Digit Verification of cas no

The CAS Registry Mumber 54423-54-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,4,2 and 3 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 54423-54:
(7*5)+(6*4)+(5*4)+(4*2)+(3*3)+(2*5)+(1*4)=110
110 % 10 = 0
So 54423-54-0 is a valid CAS Registry Number.
InChI:InChI=1/C41H39NO9/c43-40(34-21-23-35(24-22-34)42(44)45)51-41-39(49-28-33-19-11-4-12-20-33)38(48-27-32-17-9-3-10-18-32)37(47-26-31-15-7-2-8-16-31)36(50-41)29-46-25-30-13-5-1-6-14-30/h1-24,36-39,41H,25-29H2

54423-54-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name A B C 4-nitrobenzoate

1.2 Other means of identification

Product number -
Other names 2,3,4,6-Tetra-O-benzyl 1-O-p-nitrobenzoyl D-glucopyranoside

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:54423-54-0 SDS

54423-54-0Relevant articles and documents

DPPE: A convenient replacement for triphenylphosphine in the Staudinger and Mitsunobu reactions

O'Neil, Ian A.,Thompson, Stephen,Murray, Clare L.,Kalindjian, S. Barret

, p. 7787 - 7790 (2007/10/03)

DPPE has been shown to replace triphenylphosphine in the Staudinger and Mitsunobu reactions. The resulting bis(phosphine oxide) by-product is readily removed allowing for rapid and simple purification of the reaction mixture.

Tumor inhibiting saccharide conjugates

-

, (2008/06/13)

The invention relates to a method for the preparation of glycoconjugates of phosphorus amides with the general formula STR1 where the connection of the sugar with the phosphoric acid amide mustard residue, and the ifosfamide mustard residue, respectively, occurs preferably in the 1-position, and where R1 and R2 ; which can be the same or different, denote hydrogen, lower C1 -C4 alkyl or C1 -C6 haloalkyl and where as sugar there can be present mono-, di-, or polysaccharides in all existing isomeric and enantiomeric forms, wherein in a known way protected brominated sugars are conjugated with the respective phosphorus compounds, and freed of the protective residues, and to the use of said compounds as anti-tumour drugs.

Synthesis of Chiral Spiroacetals from Carbohydrates

Martin, Angeles,Salazar, Jose A.,Suarez, Ernesto

, p. 4489 - 4492 (2007/10/02)

Optically active spiroacetals are prepared from carbohydrates with an intramolecular hydrogen abstraction reaction as the key step.Both spiroacetal enantiomers are formally available from the same sugar.

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