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4447-21-6

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4447-21-6 Usage

Molecular structure

Linear alkyne

Physical state at room temperature

Colorless, flammable liquid

Boiling point

88-89°C

Uses

a. Precursor in the synthesis of various organic compounds
b. Synthesis of pharmaceuticals and polymers
c. Reagent in organic chemical reactions
d. Preparation of substituted acetylenes

Hazardous properties

a. Toxic if ingested, inhaled, or in contact with the skin
b. Causes irritation to the respiratory system and skin

Safety precautions

a. Proper handling, storage, and disposal procedures
b. Ensure safe use by following guidelines and regulations

Check Digit Verification of cas no

The CAS Registry Mumber 4447-21-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,4 and 7 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4447-21:
(6*4)+(5*4)+(4*4)+(3*7)+(2*2)+(1*1)=86
86 % 10 = 6
So 4447-21-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H6/c1-3-5-6-4-2/h1H,4H2,2H3

4447-21-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name hexa-1,3-diyne

1.2 Other means of identification

Product number -
Other names Ethyldiacetylene

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:4447-21-6 SDS

4447-21-6Relevant articles and documents

Synthesis of 7E,9Z-dodecadienyl acetate, the sex pheromone of Lobesia botrana Shiff

Chrelashvili, Z. G.,Mavrov, M. V.,Dolidze, A. V.,Voronkov, A. P.,Serebryakov, E. P.

, p. 734 - 736 (2007/10/02)

Two syntheses of 7E,9Z-dodecadienyl acetate from 1,3-butadiyne were carried out using either 2E,4Z-heptadienyl acetate or 1-bromo-3E,5Z-octadiene as the key intermediates.The latter underwent organocopper cross-coupling with the respective complementary Grignard reagents (prepared from the corresponding 1-tert-butoxy-ω-chlorohydrins) as alkylating agents.

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