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74266-80-1

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74266-80-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74266-80-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,2,6 and 6 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 74266-80:
(7*7)+(6*4)+(5*2)+(4*6)+(3*6)+(2*8)+(1*0)=141
141 % 10 = 1
So 74266-80-1 is a valid CAS Registry Number.

74266-80-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1'-Methyl-2'-butenyl)aniline

1.2 Other means of identification

Product number -
Other names 2-(1-Methyl-2-butenyl)anilin

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:74266-80-1 SDS

74266-80-1Relevant articles and documents

Synthesis of (1′S*,2R*,3R*)- and (1′S*,2R*,3S*)-N-arylsulfonyl-2-(1′-halogenethyl)-3-methylindolines and their selective toxicity against SH-SY5Y cell line

Gataullin, Rail R.,Maksimova, Marina A.,Vakhitova, Yuliya V.,Zainullina, Liana F.,Zileeva, Zulfia R.

, (2020/01/24)

N-tosyl-2- and N-tosyl-4-halogen-substituted derivatives of 2-(1-methylbut-2-en-1-yl)aniline were synthesized and their molecular iodine-mediated cyclization was investigated. The cyclization upon interaction of N-tosyl-6-methyl-2-(1-methylbut-2-en-1-yl)a

Alkenylation of anilines with dicyclopentadiene, cyclopentadiene, and piperylene

Gataullin,Kazhanova,Sagitdinov,Galyautdinov,Fatykhov,Spirikhin,Abdrakhmanov

, p. 280 - 285 (2007/10/03)

Alkenylation of anilines with dicyclopentadiene, cyclopentadiene, and piperylene in the presence of mineral acids and Lewis acids was studied.

ACID-CATALYZED RERRANGEMENT OF N-(1-METHYL-2-BUTENYL)ANILINE

Abdrakhmanov, I.B.,Sharafutdidov, V.M.,Tolstikov, G.A.

, p. 562 - 564 (2007/10/02)

The effect of the nature of the solvents and catalysts on the rerrangement of N-(1-methyl-2-butenyl)aniline was studied..The reaction is catalyzed by the hydrochlorides of aromatic amines and by Lewis acids.The nature of the solvents has an insignificant effect on the course of the rearrangement.

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