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10557-17-2

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10557-17-2 Usage

Chemical Properties

Clear Yellow Oil

Uses

Different sources of media describe the Uses of 10557-17-2 differently. You can refer to the following data:
1. A metabolite of Bupropion (B689625).
2. 1-(3-Chlorophenyl)-1,2-propanedione is a metabolite of Bupropion (B689625). Bupropion USP Related Compound E.

Check Digit Verification of cas no

The CAS Registry Mumber 10557-17-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,5 and 7 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 10557-17:
(7*1)+(6*0)+(5*5)+(4*5)+(3*7)+(2*1)+(1*7)=82
82 % 10 = 2
So 10557-17-2 is a valid CAS Registry Number.

10557-17-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-chlorophenyl)propane-1,2-dione

1.2 Other means of identification

Product number -
Other names 1,2-Propanedione,1-(3-chlorophenyl)

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:10557-17-2 SDS

10557-17-2Downstream Products

10557-17-2Relevant articles and documents

Synthesis of 1,2-diketones from β-keto nitriles via a protection-oxidative-decyanation-deprotection protocol

Liu, Yu,Yun, Xiliu,Zhang-Negrerie, Daisy,Huang, Jianhui,Du, Yunfei,Zhao, Kang

, p. 2984 - 2994 (2011/11/04)

A variety of 1,2-diketones were prepared from -keto nitriles via a three-step protocol including the protection of the ketones with methoxyamine, oxidative decyanation, and microwave-assisted deprotection in the final step. This approach provides a novel and efficient access to a wide scope of symmetric and unsymmetric 1,2-diketones using molecular oxygen as the oxidant in the decyanation process. Georg Thieme Verlag Stuttgart - New York.

New synthetic strategy for high-enantiopurity N-protected α-amino ketones and their derivatives by asymmetric hydrogenation

Sun, Tian,Hou, Guohua,Ma, Miaofeng,Zhang, Xumu

supporting information; experimental part, p. 253 - 256 (2011/04/16)

Asymmetric hydrogenation of α-dehydroamino ketones catalyzed by a rhodium-chiral phosphorus ligand complex (up to 99% ee, 1000 TON), represents an efficient approach to chiral α-amino ketones. The reduction of α-amino ketones catalyzed by palladium on carbon (Pd/C) leads to amphetamine precursors with quantitative yield and no significant enantioselectivity loss.

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