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3-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]-1-propanol, 4-nitrobenzenesulfonate is a complex organic compound featuring a 1-propanol molecule with a tert-butyldimethylsilyloxy group attached to the third carbon and a 4-nitrobenzenesulfonate group attached to the hydroxyl group. 3-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]-1-propanol, 4nitrobenzenesulfonate is notable for its role in organic synthesis and medicinal chemistry, where the tert-butyldimethylsilyloxy group serves as a protective agent to shield reactive sites from unwanted reactions, and the 4-nitrobenzenesulfonate group functions as a leaving group in substitution reactions, facilitating the formation of new chemical bonds.

220299-14-9

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  • 3-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]-1-propanol, 4-nitrobenzenesulfonate

    Cas No: 220299-14-9

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220299-14-9 Usage

Uses

Used in Organic Synthesis:
3-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]-1-propanol, 4-nitrobenzenesulfonate is used as a reagent in organic synthesis for its ability to participate in substitution reactions, where the 4-nitrobenzenesulfonate group acts as a leaving group, allowing for the formation of new chemical bonds with other molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 3-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]-1-propanol, 4-nitrobenzenesulfonate is utilized as a building block for the synthesis of more complex molecules with potential therapeutic applications. Its reactivity and structural features make it a valuable component in the development of new pharmaceutical agents.
Used in Protecting Group Chemistry:
3-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]-1-propanol, 4-nitrobenzenesulfonate is used as a protecting group in protecting group chemistry to shield functional groups from participating in unwanted side reactions during the synthesis of complex organic molecules, ensuring the desired product is obtained with minimal impurities.
Used in the Pharmaceutical Industry:
3-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]-1-propanol, 4-nitrobenzenesulfonate is used as an intermediate in the pharmaceutical industry for the synthesis of drug candidates, leveraging its reactivity and structural attributes to create molecules with specific biological activities and therapeutic potentials.

Check Digit Verification of cas no

The CAS Registry Mumber 220299-14-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,2,9 and 9 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 220299-14:
(8*2)+(7*2)+(6*0)+(5*2)+(4*9)+(3*9)+(2*1)+(1*4)=109
109 % 10 = 9
So 220299-14-9 is a valid CAS Registry Number.
InChI:InChI=1S/C15H25NO6SSi/c1-15(2,3)24(4,5)22-12-6-11-21-23(19,20)14-9-7-13(8-10-14)16(17)18/h7-10H,6,11-12H2,1-5H3

220299-14-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[tert-butyl(dimethyl)silyl]oxypropyl 4-nitrobenzenesulfonate

1.2 Other means of identification

Product number -
Other names 3-((tert-Butyldimethylsilyl)oxy)propyl 4-nitrobenzenesulfonate

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:220299-14-9 SDS

220299-14-9Upstream product

220299-14-9Downstream Products

220299-14-9Relevant articles and documents

Urokinase inhibitors

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, (2008/06/13)

Compounds having the formula are inhibitors of urokinase and are useful in the treatment of diseases in which urokinase plays a role. Also disclosed are urokinase-inhibiting compositions and a method of inhibiting urokinase in a mammal.

Ukokinase inhibitors

-

, (2008/06/13)

Compounds having the formula are inhibitors of urokinase and are useful in the treatment of diseases in which urokinase plays a role. Also disclosed are urokinase-inhibiting compositions and a method of inhibiting urokinase in a mammal.

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