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1846-68-0

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1846-68-0 Usage

Description

2-Octynal 97, also known as 2-Octanal, is an organic compound with the chemical formula C8H14O. It is a colorless to pale yellow liquid with a strong, fatty, and slightly pungent odor. It is a member of the aldehyde family and is commonly used as a building block in the synthesis of various organic compounds.

Uses

Used in Pharmaceutical Industry:
2-Octynal 97 is used as a synthetic intermediate for the production of various pharmaceutical compounds. It plays a crucial role in the synthesis of (R)and (S)-argentilactone, which are important compounds in the development of new drugs.
Used in Chemical Synthesis:
2-Octynal 97 is used as a key building block in the synthesis of various organic compounds, including natural products and complex molecules. Its unique structure allows for a wide range of chemical reactions, making it a versatile compound in the field of organic chemistry.
Used in Enantioselective Catalytic Allylation (ECA):
2-Octynal 97 is used as a starting material in the enantioselective catalytic allylation (ECA) process, which is a powerful and widely used method for the asymmetric synthesis of chiral compounds. This process allows for the selective formation of one enantiomer over the other, which is essential in the development of enantiomerically pure drugs and other chiral compounds.
Used in Ring-Closing Metathesis Pathways:
2-Octynal 97 is also used in ring-closing metathesis pathways, which are important reactions in the synthesis of cyclic compounds. These reactions involve the formation of a new carbon-carbon double bond and the closure of a ring, leading to the formation of complex cyclic structures with a high degree of selectivity and efficiency.

Check Digit Verification of cas no

The CAS Registry Mumber 1846-68-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,4 and 6 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1846-68:
(6*1)+(5*8)+(4*4)+(3*6)+(2*6)+(1*8)=100
100 % 10 = 0
So 1846-68-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H12O/c1-2-3-4-5-6-7-8-9/h8H,2-5H2,1H3

1846-68-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name oct-2-ynal

1.2 Other means of identification

Product number -
Other names oct-2-yn-al

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:1846-68-0 SDS

1846-68-0Relevant articles and documents

Rickards,Weiler

, p. 3607 (1978)

Palladium-catalyzed oxidative borylation of conjugated enynones through carbene migratory insertion: synthesis of furyl-substituted alkenylboronates

Ping, Yifan,Chang, Taiwei,Wang, Kang,Huo, Jingfeng,Wang, Jianbo

supporting information, p. 59 - 62 (2019/01/03)

A palladium-catalyzed oxidative borylation reaction of conjugated enynones is developed. This reaction represents a new method for the synthesis of furyl-substituted alkenylboronates. The reaction works well with a series of conjugated enynones. Boryl migratory insertion of the palladium carbene intermediate is proposed as the key step in these transformations.

Synthetic method for organic synthesis intermediate 2-octynaldehyde

-

Paragraph 0012; 0013; 0016; 0017; 0018 - 0021, (2018/07/30)

The invention discloses a synthetic method for the organic synthesis intermediate 2-octynaldehyde. The synthetic method comprises the following steps: adding 2-octyne-1-propyl ether and an anhydrous 2-bromopropane solution into a reaction vessel, controlling a solution temperature and a stirring speed, and carrying out a reaction; and then adding cadmium selenide powder and an anhydrous ethylene glycol carbonate solution in batches, raising the temperature, continuing the reaction, lowering the temperature, carrying out standing, subjecting the solution to layering, separating an oil layer, washing the oil layer in an anhydrous 2,5-dimethylfuran solution a plurality of times, then washing the oil layer in an anhydrous dimethyl sulphoxide solution a plurality of times, carrying out recrystallization in an anhydrous diethylene glycol solution, and then carrying out dehydration with a dehydrating agent to obtain the finished 2-octynaldehyde.

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