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(R)-2-(Benzyloxycarbonylamino)-1,4-dimethanesulfonyloxybutane is a complex organic chemical compound derived from butane, featuring a benzyloxycarbonylamino group and a dimethanesulfonyloxy group. Its unique structure, with these functional groups, suggests potential applications in peptide chemistry and as a protecting group for amino acids, as well as a leaving group in organic synthesis. (R)-2-(Benzyloxycarbonylamino)-1,4-dimethanesulfonyloxybutane may serve as a versatile building block in the synthesis of complex molecules within the field of organic chemistry.

655785-24-3

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655785-24-3 Usage

Uses

Used in Organic Chemistry:
(R)-2-(Benzyloxycarbonylamino)-1,4-dimethanesulfonyloxybutane is used as a building block for the synthesis of complex organic molecules, due to its unique functional groups that facilitate various chemical reactions and transformations.
Used in Peptide Chemistry:
In peptide chemistry, (R)-2-(Benzyloxycarbonylamino)-1,4-dimethanesulfonyloxybutane is used as a protecting group for amino acids, which is crucial for the selective synthesis of peptides and proteins.
Used in Medicinal Chemistry:
(R)-2-(Benzyloxycarbonylamino)-1,4-dimethanesulfonyloxybutane may be utilized in the development of pharmaceuticals, given its potential to be incorporated into drug molecules, enhancing their stability, solubility, or bioavailability.
Used in Chemical Synthesis as a Leaving Group:
The dimethanesulfonyloxy group in (R)-2-(Benzyloxycarbonylamino)-1,4-dimethanesulfonyloxybutane makes it a suitable leaving group in organic synthesis, which can be exploited in reactions such as nucleophilic substitutions or eliminations to form new chemical bonds.
Used in the Synthesis of Chiral Compounds:
Due to its chiral center, (R)-2-(Benzyloxycarbonylamino)-1,4-dimethanesulfonyloxybutane can be employed in the synthesis of enantiomerically pure compounds, which are essential in various applications, including pharmaceuticals and agrochemicals, where stereochemistry plays a critical role in biological activity.

Check Digit Verification of cas no

The CAS Registry Mumber 655785-24-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,5,7,8 and 5 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 655785-24:
(8*6)+(7*5)+(6*5)+(5*7)+(4*8)+(3*5)+(2*2)+(1*4)=203
203 % 10 = 3
So 655785-24-3 is a valid CAS Registry Number.

655785-24-3SDS

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 [(3R)-4-methylsulfonyloxy-3-(phenylmethoxycarbonylamino)butyl] methanesulfonate

1.2 Other means of identification

Product number -
Other names (R)-2-(((Benzyloxy)carbonyl)amino)butane-1,4-diyl dimethanesulfonate

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:655785-24-3 SDS

655785-24-3Downstream Products

655785-24-3Relevant academic research and scientific papers

A kind of optical active pharmaceutical process for the preparation of intermediates

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Paragraph 0052; 0053, (2016/10/17)

The invention relates to a preparation method of an optical active compound, represented by formula I, or a hydrochloride of the optical active compound by taking a compound with optical activity as a starting material. Raw materials of the preparation method are cheap and easily available; no splitting is needed; the whole technological operation is simple and convenient; cost is low; pollution on environment is less; and the preparation method is suitable for industrialized production. In the formula I, n is 1 or 2 or 3.

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