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16387-55-6

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16387-55-6 Usage

General Description

2-Octynal diethyl acetal 98 is a chemical compound with the formula C10H18O2. It is a colorless liquid with a strong, sweet, floral odor. It is commonly used as a flavor and fragrance ingredient in cosmetics, personal care products, and household cleaners. This chemical is known for its low toxicity and is considered safe for use in consumer products when used as directed. It is also used as a solvent and as a starting material in organic synthesis. 2-Octynal diethyl acetal 98 is typically used as a flavoring agent in food products and as a fragrance ingredient in perfumes and colognes.

Check Digit Verification of cas no

The CAS Registry Mumber 16387-55-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,3,8 and 7 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 16387-55:
(7*1)+(6*6)+(5*3)+(4*8)+(3*7)+(2*5)+(1*5)=126
126 % 10 = 6
So 16387-55-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H22O2/c1-4-7-8-9-10-11-12(13-5-2)14-6-3/h12H,4-9H2,1-3H3

16387-55-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1-diethoxyoct-2-yne

1.2 Other means of identification

Product number -
Other names 1,1-Diethoxy-2-octyne

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:16387-55-6 SDS

16387-55-6Relevant articles and documents

Neighbouring-group influence on the ring opening of some 2-alkyl-1,1,2-tribromocyclopropanes under phase-transfer conditions

Sydnes, Leiv K.,Alnes, Karl F. S.,Erdogan, Natalia

, p. 1737 - 1749 (2007/10/03)

Several 2-alkyl-1,1,2-tribromocyclopropanes were treated with sodium hydroxide and ethanol under phase-transfer conditions. Ring opening gave mixtures of the corresponding acetylenic diethyl ketals and acetals. When the steric bulk of the alkyl substituent was increased acetal formation dominated, and in the case of 1,1,2-tribromo-2-(tert-butyl)cyclopropane, the acetal was formed as the only product. Springer-Verlag 2005.

The Stereoselective Synthesis of Ethyl 2(E),4(Z)-Decadienoate

Byrne, Brian,Lawter, Louise M. Lafleur,Wengenroth, Karl J.

, p. 2607 - 2609 (2007/10/02)

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