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1076-99-9

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1076-99-9 Usage

General Description

The chemical 4-ALLYL-BENZOIC ACID, also known as 4-allylbenzoic acid, is an organic compound with the chemical formula C10H10O2. It is a white crystalline powder that is only slightly soluble in water but soluble in organic solvents. 4-ALLYL-BENZOIC ACID is commonly used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and organic compounds. It is also used as a building block in the production of polymers and resins. Additionally, 4-allyl-benzoic acid has been studied for its potential anti-inflammatory and anticancer properties, making it an interesting compound for further research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 1076-99-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1076-99:
(6*1)+(5*0)+(4*7)+(3*6)+(2*9)+(1*9)=79
79 % 10 = 9
So 1076-99-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H10O2/c1-2-3-8-4-6-9(7-5-8)10(11)12/h2,4-7H,1,3H2,(H,11,12)

1076-99-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-prop-2-enylbenzoic acid

1.2 Other means of identification

Product number -
Other names 4-Allyl-benzoic acid

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:1076-99-9 SDS

1076-99-9Relevant articles and documents

Cross-Coupling Reactions of Aryldiazonium Salts with Allylsilanes under Merged Gold/Visible-Light Photoredox Catalysis

Akram, Manjur O.,Mali, Pramod S.,Patil, Nitin T.

supporting information, p. 3075 - 3078 (2017/06/23)

A method for the cross-coupling reactions of aryldiazonium salts with trialkylallylsilanes via merged gold/photoredox catalysis is described. The reaction is proposed to proceed through a photoredox-promoted generation of an electrophilic arylgold(III) intermediate that undergoes transmetalation with allyltrimethylsilane to form allylarenes.

Synthesis of C2-C3′N-linked macrocyclic taxoids. Novel docetaxel analogues with high tubulin activity

Querolle, Olivier,Dubois, Jo?lle,Thoret, Sylviane,Roussi, Fanny,Guéritte, Fran?oise,Guénard, Daniel

, p. 5937 - 5944 (2007/10/03)

Novel C2-C3′N-linked macrocyclic taxoids 4 bearing an aromatic ring at position C2 were synthesized. These compounds, tethered between N3′ and the C2-aromatic ring at the ortho, meta, or para position, were constructed by ring-closing metathesis. The para

Cyclic Siloxanes with Mesogenic Side Groups

Kreuzer, F.-H.,Andrejewski, D.,Haas, W.,Haeberle, N.,Riepl, G.,Spes, P.

, p. 345 - 378 (2007/10/02)

Cyclic liquid crystalline siloxanes (CLCS) are optical uniaxial positive (SA, N) and negative (N*) materials in accordance with calamitic structures.X-Ray measurements indicate, that the distances of SA layers correspond with the length of the monomer unit.In the case of mesogens with high polarity the distance is 1.7 fold the length of the monomer unit.A bundle model is proposed for CLC siloxanes.

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