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6906-64-5

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6906-64-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6906-64-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,0 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6906-64:
(6*6)+(5*9)+(4*0)+(3*6)+(2*6)+(1*4)=115
115 % 10 = 5
So 6906-64-5 is a valid CAS Registry Number.

6906-64-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-allyloxy-1,2-dimethoxybenzene

1.2 Other means of identification

Product number -
Other names 1-Allyloxy-3,4-dimethoxy-benzol

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:6906-64-5 SDS

6906-64-5Relevant articles and documents

CELLULOSIC COMPLEX AND APPLICATIONS THEREOF

-

Page/Page column 6-7; 11-12, (2020/10/20)

The present invention provides a polysaccharide supported fluorinating agents which can be used in fluorination reactions. The invention particularly describes a new bacterial cellulose supported tetra-n-butyl ammonium fluoride complex [NBu4(Bac-Cell-OH)F] which is stable and non-hygroscopic. The invention further relates to a process for fluorination using the [NBu4(Bac-Cell-OH)F] complex.

Total synthesis of (-)-Haouamine B pentaacetate and structural revision of haouamine B

Momoi, Yuichi,Okuyama, Kei-Ichiro,Toya, Hiroki,Sugimoto, Kenji,Okano, Kentaro,Tokuyama, Hidetoshi

supporting information, p. 13215 - 13219 (2015/01/09)

The enantiocontrolled total synthesis of (-)-haouamine B pentaacetate was accomplished via an optically active indane-fused β-lactam, which was prepared by a newly developed Friedel-Crafts reaction. Subsequent cleavage of the β-lactam and an intramolecular McMurry coupling reaction provided the core indane-fused tetrahydropyridine, which led to the elucidation of the structure, as proposed by Trauner and Zuba.

Ring-closing metathesis for the synthesis of benzo-fused bicyclic compounds

Van Otterlo, Willem A.L.,Ngidi, E. Lindani,Coyanis, E. Mabel,De Koning, Charles B.

, p. 311 - 313 (2007/10/03)

Ring-closing metathesis (RCM) was used to synthesise five 4H-chromenes, a naphthol and an indenol. These are the first examples of RCM applied to the synthesis of such benzo-fused bicyclic compounds.

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