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2,3,4,6-tetrakis(benzyloxy)-5-hydroxy-N,N-dimethylhexanamide, also known by its non-preferred name, is a complex organic chemical compound characterized by a hexanamide backbone with four benzyloxy groups and a hydroxy group. Additionally, it features two methyl groups attached to the amine functional group. 2,3,4,6-tetrakis(benzyloxy)-5-hydroxy-N,N-dimethylhexanamide (non-preferred name) is recognized for its role as a protecting group in organic synthesis and medicinal chemistry, facilitating selective reactions without compromising the amine functionality. Its versatility positions it as a valuable asset in the pharmaceutical industry and in the creation of novel chemical entities.

13096-63-4

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13096-63-4 Usage

Uses

Used in Organic Synthesis:
2,3,4,6-tetrakis(benzyloxy)-5-hydroxy-N,N-dimethylhexanamide (non-preferred name) is used as a protecting group for amines in organic synthesis, allowing chemists to perform selective reactions on other functional groups present in the molecule without the amine reacting. This selective protection is crucial for complex molecule assembly and the synthesis of intricate organic compounds.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2,3,4,6-tetrakis(benzyloxy)-5-hydroxy-N,N-dimethylhexanamide (non-preferred name) serves a similar purpose as in organic synthesis, acting as a protecting group for amines. This is particularly important in the development of new pharmaceuticals, where the selective modification of certain functional groups is necessary to explore the structure-activity relationship of potential drug candidates.
Used in Pharmaceutical Industry:
2,3,4,6-tetrakis(benzyloxy)-5-hydroxy-N,N-dimethylhexanamide (non-preferred name) is utilized in the pharmaceutical industry for the development of new drugs. Its role as a protecting group enables the synthesis of complex molecular structures with specific biological activities, contributing to the advancement of medicinal agents with improved efficacy and selectivity.
Used in the Development of New Chemical Compounds:
2,3,4,6-tetrakis(benzyloxy)-5-hydroxy-N,N-dimethylhexanamide (non-preferred name) is also used in the development of new chemical entities, where its protective properties allow for the exploration of novel chemical space. The ability to selectively modify molecules while protecting the amine group opens up new avenues for the creation of compounds with unique properties and potential applications across various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 13096-63-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,9 and 6 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13096-63:
(7*1)+(6*3)+(5*0)+(4*9)+(3*6)+(2*6)+(1*3)=94
94 % 10 = 4
So 13096-63-4 is a valid CAS Registry Number.

13096-63-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-hydroxy-N,N-dimethyl-2,3,4,6-tetrakis(phenylmethoxy)hexanamide

1.2 Other means of identification

Product number -
Other names 2,3,4,6-Tetra-O-benzyl-N,N-dimethyl-D-gluconamid

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:13096-63-4 SDS

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