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94011-49-1

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94011-49-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94011-49-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,0,1 and 1 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 94011-49:
(7*9)+(6*4)+(5*0)+(4*1)+(3*1)+(2*4)+(1*9)=111
111 % 10 = 1
So 94011-49-1 is a valid CAS Registry Number.

94011-49-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl 2-phenacylpropanedioate

1.2 Other means of identification

Product number -
Other names diethyl phenacylmalonate

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:94011-49-1 SDS

94011-49-1Relevant articles and documents

Cu(OAc)2-Triggered Cascade Reaction of Malonate-Tethered Acyl Oximes with Indoles, Indole-2-alcohols, and Indole-2-carboxamides

Mao, Peng-Fei,Zhou, Li-Jin,Zheng, An-Qi,Miao, Chun-Bao,Yang, Hai-Tao

supporting information, p. 3153 - 3157 (2019/05/10)

A Cu(OAc)2-promoted cascade reaction of malonate-tetherd acyl oximes with indoles, indole-2-alcohols, or indole-2-carboxmides provides facile access to polysubstituted 3-pyrrolin-2-ones. The reaction features the generation of two adjacent elec

Copper-Catalyzed Dehydrogenative Diels-Alder Reaction

Jiang, Bing,Liang, Qiu-Ju,Han, Yu,Zhao, Meng,Xu, Yun-He,Loh, Teck-Peng

supporting information, p. 3215 - 3219 (2018/06/11)

A practical and effective copper-catalyzed dehydrogenative Diels-Alder reaction of gem-diesters and ketone with dienes has been established. The active dienophiles were generated in situ via a radical-based dehydrogenation process, which reacted with a wide variety of dienes to afford various polysubstituted cyclohexene derivatives in good to excellent yields.

Synthesis of vinyldihydropyran by cooperative catalysis

Vulovi?, Bojan,Mari?, Ivana,Matovi?, Radomir,Saicí?, Radomir N.

, p. 1335 - 1343 (2017/01/24)

Δ5-Unsaturated aldehydes with a suitably positioned allylic halide, or phosphate, leaving group undergo doubly-catalyzed cyclization to give dihydropyran derivatives. The cyclization proceeds under the synergetic action of diazabicycloundecene and Pd(PPh3)4. This type of transformation was also accomplished with an aryl ketone.

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