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Factory Supply 2-Bromo-5-fluorophenol
Cas No: 147460-94-4
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Ality Chemical Corporation
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2-Propenoic acid,3-[[(2E)-3-phenyl-2-propen-1-yl]oxy]-, methyl ester, (2E)-
Cas No: 147460-94-4
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Zibo Hangyu Biotechnology Development Co., Ltd
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2-Propenoic acid,3-[[(2E)-3-phenyl-2-propen-1-yl]oxy]-, methyl ester, (2E)-
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147460-94-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 147460-94-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,4,6 and 0 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 147460-94:
(8*1)+(7*4)+(6*7)+(5*4)+(4*6)+(3*0)+(2*9)+(1*4)=144
144 % 10 = 4
So 147460-94-4 is a valid CAS Registry Number.

InChI:InChI=1/C7H3F13O4/c8-2(9,1-21)22-3(10,11)4(12,13)23-5(14,15)6(16,17)24-7(18,19)20/h21H,1H2

147460-94-4SDS

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	(2E)-methyl 3-(cinnamyloxy)acrylate

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

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Service hours	Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:147460-94-4 SDS

147460-94-4Upstream product

147460-94-4Downstream Products

147460-94-4Relevant articles and documents

Transition-metal-mediated cascade reactions: The water-accelerated carboalumination-Claisen rearrangement-carbonyl addition reaction

Wipf, Peter,Waller, David L.,Reeves, Jonathan T.

, p. 8096 - 8102 (2007/10/03)

A three-step cascade reaction involving a water-accelerated catalytic carboalumination, a Claisen rearrangement, and a nucleophilic carbonyl addition converts terminal alkynes and allyl vinyl ethers into allylic alcohols containing up to three contiguous asymmetric carbon centers. Stoichiometric quantities of water as an additive increase the rate of the [3,3] sigmatropic rearrangement as well as the diastereoselectivity of the carbonyl addition process. Reaction products contain 1,6-diene functionalities that are readily cyclized to substituted cyclopentenes. An extension of this methodology to a sequence involving a [1,3] sigmatropic shift was feasible with a cyclopropylmethyl vinyl ether substrate.

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CAS

147460-94-4