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70628-24-9

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70628-24-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70628-24-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,6,2 and 8 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 70628-24:
(7*7)+(6*0)+(5*6)+(4*2)+(3*8)+(2*2)+(1*4)=119
119 % 10 = 9
So 70628-24-9 is a valid CAS Registry Number.

70628-24-9SDS

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 ethyl 4-[2-(diethylamino)ethoxy]benzoate

1.2 Other means of identification

Product number -
Other names ethyl 4-(2-diethylaminoethyloxy)benzoate

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:70628-24-9 SDS

70628-24-9Relevant articles and documents

Synthesis of several phenoxymethylphenyl derivatives with local-anesthetic activity

Rudinger-Adler,Buchi

, p. 591 - 594 (2007/10/06)

Several 4-phenoxymethyl-procaine derivatives were synthetised in order to investigate the influence of the intermediate chain on the activity. By replacing the CH2-CH2-group in fomocain by a COO-group the authors succeeded in doubling the efficacy of this local anesthetic. The type and position of the hetero atoms, N, S and O, in the intermediate chain of the procain, xylocaine, cinchocaine and phenoxymethyl-procaine series, have in each of these series quite a different effect due to the structureal specificity of the remaining part of the molecule. Other examples confirm the significance of the ester group in the intermediate chain for the liposolubility and reactivity. In ketones these properties are altered unfavourably.

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