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78330-02-6

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78330-02-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78330-02-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,3,3 and 0 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 78330-02:
(7*7)+(6*8)+(5*3)+(4*3)+(3*0)+(2*0)+(1*2)=126
126 % 10 = 6
So 78330-02-6 is a valid CAS Registry Number.

78330-02-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 4-hydroxy-3-(morpholin-4-ylmethyl)benzoate

1.2 Other means of identification

Product number -
Other names BENZOIC ACID,4-HYDROXY-3-MORPHOLINOMETHYL-,ETHYL ESTER

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:78330-02-6 SDS

78330-02-6Downstream Products

78330-02-6Relevant articles and documents

Cu(II)-Catalyzed ortho-Selective Aminomethylation of Phenols

Dai, Jin-Ling,Shao, Nan-Qi,Zhang, Jin,Jia, Run-Ping,Wang, Dong-Hui

supporting information, p. 12390 - 12393 (2017/09/23)

A Cu(II)-catalyzed ortho-selective functionalization of free phenols with trifluoroborates to afford Csp2-Csp3 coupling products under mild conditions has been developed. A variety of functional groups on the phenol and the potassium aminomethyltrifluoroborate substrates were found compatible, furnishing the corresponding products in moderate to excellent yields. A single-electron transfer radical coupling mechanism involving a six-membered transition state is proposed to rationalize the high levels of ortho-selectivity in the reaction. This protocol provides straightforward access to ortho-aminomethyl-substituted phenols, unnatural amino acids and other bioactive small molecules.

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