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1H-Indole, 1-ethenyl-4,5,6,7-tetrahydro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51050-85-2

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51050-85-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51050-85-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,0,5 and 0 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 51050-85:
(7*5)+(6*1)+(5*0)+(4*5)+(3*0)+(2*8)+(1*5)=82
82 % 10 = 2
So 51050-85-2 is a valid CAS Registry Number.

51050-85-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-vinyl-4,5,6,7-tetrahydroindole

1.2 Other means of identification

Product number -
Other names 1-vinylpyrrole-4,5,6,7-tetrahydroindole

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:51050-85-2 SDS

51050-85-2Relevant academic research and scientific papers

PYRROLES FROM KETOXIMES AND ACETYLENE. 22. DIHALOETHANES IN PLACE OF ACETYLENE IN REACTIONS WITH CYCLOHEXANONE OXIME

Mikhaleva, A. I.,Trofimov, B. A.,Vasil'ev, A. N.,Komarova, G. A.,Skorobogatova, V. I.

, p. 920 - 923 (1982)

4,5,6,7-Tetrahydroindole and its 1-vinyl derivative were obtained in overall yields of 30-60percent by the reaction of cyclohexanone oxime with 1,2-dichloro- and 1,2-dibromoethane in the MOH-dimethyl sulfoxide (DMSO) superbase system (M = K, Na, Li).Nucle

PYRROLES FROM KETOXIMES AND ACETYLENE. CONDITIONS OF REACTION OF CYCLOHEXANONE OXIME WITH VINYL HALIDES IN SUPERBASIC MEDIA

Aliev, I. A.,Mikhaleva, A. I.,Bairamova, S. Kh.,Akhmedov, E. I.

, p. 433 - 435 (2007/10/02)

4,5,6,7-Tetrahydroindole and its N-vinyl derivatives were synthesized with an overall yield of up to 60percent by the reaction of cyclohexanone oxime with vinyl halides (CH2=CHX, where X = Cl, Br) in a MOH (M = Na, K)-polar aprotic solvent system at 84-140 deg C and atmospheric pressure.

PYRROLES FROM KETOXIMES AND ACETYLENE XVII. STUDY OF THE CONDITIONS FOR THE REACTION OF CYCLOHEXANONE OXIME WITH ACETYLENE IN SUPERBASIC MEDIA

Mikhaleva, A. I.,Vasil'ev, A. N.,Trofimov, B. A.

, p. 1763 - 1766 (2007/10/02)

The principal trends in the effects of the solvent and the concentration and nature of the hydroxide (MOH, M = Li, Na, K, Rb, Cs, Bu4N) on the yield and ratio of 4,5,6,7-tetrahydroindole and its 1-vinyl derivative, obtained from cyclohexanone oxime and acetylene in a single stage were investigated.

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