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146195-71-3

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146195-71-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 146195-71-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,1,9 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 146195-71:
(8*1)+(7*4)+(6*6)+(5*1)+(4*9)+(3*5)+(2*7)+(1*1)=143
143 % 10 = 3
So 146195-71-3 is a valid CAS Registry Number.

146195-71-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Bicyclo[2.2.1]hept-2-yl-propynal

1.2 Other means of identification

Product number -
Other names -

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:146195-71-3 SDS

146195-71-3Upstream product

146195-71-3Downstream Products

146195-71-3Relevant articles and documents

ALKYNYLHALOCARBENES. 2. GENERATION OF (ALKYN-1-YL)CHLOROCARBENES BY BASIC SOLVOLYSIS OF 1,1-DICHLORO-2-ALKYNES AND THEIR REACTION WITH OLEFINS: SYNTHESIS OF 1-CHLORO-1-ALKYNYLCYCLOPROPANES

Shavrin, K. N.,Krylova, I. V.,Dolgii, I. E.,Nefedov, O. M.

, p. 885 - 891 (1992)

1,1-Dichloro-2-alkynes R1CCCHCl2 (4a-g: R1=Me, n-Pr, c-Pr, t-Bu, Ad, Nor, Ph) were synthesized with yields of 50-75percent by chlorination with PCl5 of formylacetylenes (3a-g), prepared by oxidation of propargyl alcohols (1a-d) with CrO3*Py*HCl complex or acidolysis of propargyl acetals (2a-c) in the presence of catalytic quantities of pyridine; the corresponding alkynylchlorocarbenes, R1CCCCl (5a-g) were generated from them with powdered KOH in a two-phase system or t-BuOK. The latter were trapped by olefins with formation of 1-chloro-1-alkynylcyclopropanes (6a-t) with yields of up to 90percent.Keywords: alkynylchlorocarbenes, 1,1-dichloro-2-alkynes, basic solvolysis, interphase catalysis, 1-chloro-1-alkynylcyclopropanes.

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