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16635-10-2

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16635-10-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16635-10-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,6,3 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 16635-10:
(7*1)+(6*6)+(5*6)+(4*3)+(3*5)+(2*1)+(1*0)=102
102 % 10 = 2
So 16635-10-2 is a valid CAS Registry Number.

16635-10-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-chlorophenyl)-1-(2-hydroxy-5-methylphenyl)prop-2-en-1-one

1.2 Other means of identification

Product number -
Other names 1-(p-chlorophenyl)-3-(2-hydroxy-5-methylphenyl)prop-1-en-3-one

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:16635-10-2 SDS

16635-10-2Relevant articles and documents

Iodine-mediated direct synthesis of 3-iodoflavones

Patil, Avinash M.,Kamble, Dayanand A.,Lokhande, Pradeep D.

, p. 1299 - 1307 (2018/04/05)

Molecular iodine has been used for the regioselective, one pot, direct synthesis of 3-iodoflavones from 2′-allyloxy chalcones, 2′-hydroxy chalcones and flavones. Allyl deprotection, cyclization dehydrogenation and α-iodination of 2′-allyloxychalcones has been achieved in a single step to offer 3-iodoflavones.

Absorption and fluorescent studies of 3-hydroxychromones

Khanna, Radhika,Kumar, Ramesh,Dalal, Aarti,Kamboj, Ramesh C.

, p. 1159 - 1163 (2015/10/20)

The synthesis and spectral studies of variously substituted 3-hydroxychromones have been carried out. A key relationship between the structural motif of synthesized 3-hydroxychromones (3-HCs) and their fluorescent properties was found. The chromones substituted with electron-donating group at 4′-position expressed the red shift of the N and T band and also exhibited the increased fluorescent intensity ratio while the chromones with electron-withdrawing group showed the blue shift of the N and T band. Therefore, these 3-HCs may behave as the possible fluorescent probes.

Synthesis of some new pyrimidines and isoxazolines and their pharmacological activity

Basawaraj, Raga,Hassappa, Ravi,Chillargi, Neelavathi,Noola, Shivanand

experimental part, p. 253 - 256 (2011/12/14)

The condensation of 5-methyl-2-hydroxy acetophenone 1 with different aromatic aldehydes in anhyd ethanol in presence of strong alkali gave 1-(5′-methyl-2′-hydroxy phenyl-1′-yl)-3-substituted arylidene-2-propen-1-ones (2a-d). Compounds (2a-d) underwent cyc

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