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214541-54-5

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214541-54-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 214541-54-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,4,5,4 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 214541-54:
(8*2)+(7*1)+(6*4)+(5*5)+(4*4)+(3*1)+(2*5)+(1*4)=105
105 % 10 = 5
So 214541-54-5 is a valid CAS Registry Number.

214541-54-5SDS

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 ethyl 2-methyl-3-(3-indolyl)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

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

More Details:214541-54-5 SDS

214541-54-5Relevant articles and documents

Control of the Bacterial Wilt of Tomato Plants by a Derivative of 3-Indolepropionic Acid Based on Selective Actions on Ralstonia solanacearum

Matsuda, Kazuhiko,Toyoda, Hideyoshi,Nishio, Hitomi,Nishida, Takatsugu,Dohgo, Mitsue,Bingo, Miki,Matsuda, Yoshinori,Yoshida, Satoshi,Harada, Satoshi,Tanaka, Hiroshi,Komai, Koichiro,Ouchi, Seiji

, p. 4416 - 4419 (1998)

3-Indolepropionic acid (IPA)-related compounds having a benzo[b]thiophene or an indazole ring and derivatives having various substituents in the propionic acid moieties were tested for their antibacterial activity against Ralstonia solanacearum. Substitution of the indole ring for other aromatic rings resulted in lowered activity, whereas addition of a methyl or a trifluoromethyl group to the propionic acid moiety had little effect. Of the derivatives, 3-(3-indolyl)butanoic acid (3-IBA) was as active as IPA, exhibiting a 10-fold higher activity with the S configuration than with the R configuration. In contrast with the strong phytotoxicity of IPA, 3-IBA was able to suppress bacterial wilt without affecting the growth of tomato plants.

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