174064-02-9

Basic information

• Product Name: 5-(TRIETHYLSILYL)-4-PENTYN-1-OL
• Synonyms: 4-Triethylsilyl-4-pentyn-1-ol;5-(TRIETHYLSILYL)-4-PENTYN-1-OL;TIMTEC-BB SBB009025;5-TRIETHYLSILYL-4-PENTYN-1-OL, 97+%;5-(triethylsilyl)pent-4-yn-1-ol
• CAS NO: 174064-02-9
• Molecular Formula: C₁₁H₂₂OSi
• Molecular Weight: 198.38
• Mol File: 174064-02-9.mol

Chemical Properties

• Boiling Point: 97 °C
• Flash Point: 105.3 °C
• Appearance: clear colorless to pale yellow liquid
• Density: 0.86
• Vapor Pressure: 0.00341mmHg at 25°C
• Refractive Index: 1.453
• CAS DataBase Reference: 5-(TRIETHYLSILYL)-4-PENTYN-1-OL(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(TRIETHYLSILYL)-4-PENTYN-1-OL(174064-02-9)
• EPA Substance Registry System: 5-(TRIETHYLSILYL)-4-PENTYN-1-OL(174064-02-9)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 174064-02-9(Hazardous Substances Data)

Usage

Chemical Properties

Clear colorless to pale yellow liquid

InChI:InChI=1/C11H22OSi/c1-4-13(5-2,6-3)11-9-7-8-10-12/h12H,4-8,10H2,1-3H3

Upstream product

• 994-30-9 triethylsilyl chloride 
• 5390-04-5 pent-1-yn-5-ol 

Downstream Products

• 929619-32-9 11-(adamantan-1-ylmethoxy)-1,3,4,5-tetrakis-benzyloxy-undec-7-yne-2,6-dione 
• 850887-96-6 (1S)-2,3,4,6-tetra-O-benzyl-1-C-[5-(adamantan-1-yl-methoxy)-pent-1-ynyl]-1-deoxynojirimycin 
• 929619-25-0 (1S)-2,3,4,6-tetra-O-benzyl-N-butyl-1-C-[5-(adamantan-1-yl-methoxy)-pent-1-ynyl]-1-deoxynojirimycin 
• 1420012-89-0 C₁₇H₂₆BrNOSi 
• 1189758-87-9 4-dimethylamino-1-[3-(1H-indol-3-yl)propyl]-4-phenylcyclohexanol 

Relevant articles and documents

Synthesis of the polyketide moiety of the jamaicamides

[Figure presented] Isolated from the Jamaican cyanobacterium Lyngbya majuscula, the jamaicamides are unique, mixed polyketide-peptides reported to be sodium channel blockers. The polyketide moiety contains an (E)-chloroolefin, an undetermined methyl stere

Development of adamantan-1-yl-methoxy-functionalized 1-deoxynojirimycin derivatives as selective inhibitors of glucosylceramide metabolism in man

(Chemical Equation Presented) In this article, we present a straightforward synthesis of adamantan-1-yl-methoxy-functionalized 1-deoxynojirimycin derivatives. The used synthetic routes are flexible and can be used to create a wide variety of lipophilic mo