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62551-73-9

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62551-73-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62551-73-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,5,5 and 1 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 62551-73:
(7*6)+(6*2)+(5*5)+(4*5)+(3*1)+(2*7)+(1*3)=119
119 % 10 = 9
So 62551-73-9 is a valid CAS Registry Number.

62551-73-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-oxo-2-(4-bromophenyl)acetyl chloride

1.2 Other means of identification

Product number -
Other names 4-Bromphenylglyoxylsaeurechlorid

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:62551-73-9 SDS

62551-73-9Relevant articles and documents

Non-Bonding 1,4-Sulphur-Oxygen Interaction Governs the Reactivity of α-Ketothioesters in Triphenylphosphine-Catalyzed Cyclization with Acetylenedicarboxylates

Bankura, Abhijit,Saha, Jayanta,Maity, Rajib,Das, Indrajit

supporting information, p. 1014 - 1021 (2020/12/31)

α-Ketothioesters undergo triphenylphosphine (PPh3)-catalyzed cyclization with acetylenedicarboxylate esters smoothly, in contrast to α-ketooxoesters which require more drastic conditions with the limited substrate scope. The reaction works well

N-Heterocyclic Carbene-Catalyzed Umpolung of Alkynyl 1,2-Diketones

Kong, Xiangwen,Zhang, Guoxiang,Yang, Shuang,Liu, Xiaozhi,Fang, Xinqiang

, p. 2729 - 2734 (2017/08/23)

The umpolung of alkynyl 1,2-diketones via N-heterocyclic carbene (NHC) catalysis was achieved for the first time, allowing the rapid access to a large variety of synthetically and pharmaceutically important α-pyrones under very mild conditions. A completely new NHC-catalyzed umpolung pattern involving an O-acylated allenolate as the key intermediate was proposed. Moreover, an unprecedented reaction pathway, featured by a series of group migrations and new bond formation, was postulated to demonstrate the formation of the products. (Figure presented.).

C?H Insertion as a Key Step to Spiro-Oxetanes, Scaffolds for Drug Discovery

Nicolle, Simon M.,Nortcliffe, Andrew,Bartrum, Hannah E.,Lewis, William,Hayes, Christopher J.,Moody, Christopher J.

supporting information, p. 13623 - 13627 (2017/09/13)

A new route to spiro-oxetanes, potential scaffolds for drug discovery, is described. The route is based on the selective 1,4-C?H insertion reactions of metallocarbenes, generated from simple carbonyl precursors in flow or batch mode, to give spiro-β-lacto

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