Welcome to LookChem.com Sign In|Join Free
  • or
5-[(tert-Butyldimethylsilyl)oxy]pentanal is a chemical compound with the molecular formula C12H26O2Si. It is a silyl enol ether that serves as a protecting group for aldehydes and ketones in organic synthesis. The tert-butyldimethylsilyl (TBS) group shields the aldehyde functional group, preventing unwanted reactions or side reactions during subsequent chemical reactions. 5-[(tert-Butyldimethylsilyl)oxy]pentanal is widely used in the production of pharmaceuticals, agrochemicals, and the synthesis of complex natural products. The TBS protecting group can be easily removed under mild conditions, making 5-[(tert-Butyldimethylsilyl)oxy]pentanal a versatile and valuable tool in organic synthesis.

87184-80-3

Post Buying Request

87184-80-3 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

87184-80-3 Usage

Uses

Used in Pharmaceutical Industry:
5-[(tert-Butyldimethylsilyl)oxy]pentanal is used as a protecting group for aldehydes and ketones in the synthesis of pharmaceuticals. The TBS group provides protection for the aldehyde functional group, allowing for selective reactions and preventing unwanted side reactions. This ensures the purity and yield of the final product, contributing to the development of effective and safe medications.
Used in Agrochemical Industry:
5-[(tert-Butyldimethylsilyl)oxy]pentanal is used as a protecting group in the synthesis of agrochemicals. The TBS group protects the aldehyde functional group, enabling selective reactions and avoiding side reactions that could lead to impurities or reduced yields. This ensures the production of high-quality agrochemicals with desired properties and minimal environmental impact.
Used in Synthesis of Complex Natural Products:
5-[(tert-Butyldimethylsilyl)oxy]pentanal is used as a protecting group in the synthesis of complex natural products. The TBS group shields the aldehyde functional group, allowing for selective reactions and preventing side reactions that could complicate the synthesis process. This facilitates the production of complex natural products with high purity and yield, contributing to the development of novel therapeutic agents and other applications.
Used in Organic Synthesis:
5-[(tert-Butyldimethylsilyl)oxy]pentanal is used as a versatile protecting group in various organic synthesis applications. The TBS group provides protection for the aldehyde functional group, enabling selective reactions and preventing unwanted side reactions. The mild conditions required for the removal of the TBS group make it a valuable tool for chemists, allowing for the synthesis of a wide range of organic compounds with high purity and yield.

Check Digit Verification of cas no

The CAS Registry Mumber 87184-80-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,1,8 and 4 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 87184-80:
(7*8)+(6*7)+(5*1)+(4*8)+(3*4)+(2*8)+(1*0)=163
163 % 10 = 3
So 87184-80-3 is a valid CAS Registry Number.

87184-80-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-[tert-butyl(dimethyl)silyl]oxypentanal

1.2 Other means of identification

Product number -
Other names 5-[(1,1-dimethylethyl)dimethylsilyloxy]pentanal

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:87184-80-3 SDS

87184-80-3Upstream product

87184-80-3Relevant academic research and scientific papers

Aromatization of 2,2,5-trialkyl-substituted 2,5-dihydrofurans and factors affecting their stabilization

Sharipov, Bulat T.,Davidova, Anna N.,Valeev, Farid A.

, p. 403 - 410 (2018/06/11)

[Figure not available: see fulltext.] We demonstrate that the synthesis of 5-methoxy-2,2,5-trialkyl-substituted 2,5-dihydrofurans containing unprotected hydroxymethyl group at the C-2 position involves aromatization via fragmentation involving С–С bond cleavage, resulting in the formation of 2,5-disubstituted furans and carbonyl compounds. 2,5-Dihydrofurans bearing an ester group at the С-2 position were stable. It was found that 2,2,5-trialkyl-substituted 2,5-dihydrofurans containing a hydroxymethyl or carbonyl group in the side chain could aromatize through auto-oxidation, which was facilitated by adjacent functional groups (sulfo- or pivaloyl groups).

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 87184-80-3