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6500-63-6

6500-63-6

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6500-63-6 Usage

Chemical Properties

Yellow Crystals

Check Digit Verification of cas no

The CAS Registry Mumber 6500-63-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,0 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6500-63:
(6*6)+(5*5)+(4*0)+(3*0)+(2*6)+(1*3)=76
76 % 10 = 6
So 6500-63-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H12O3/c1-15-11-7-4-6-10(9-11)5-2-3-8-12(13)14/h2-9H,1H3,(H,13,14)/b5-2+,8-3-

6500-63-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(3-Methoxyphenyl)penta-2,4-dienoic acid

1.2 Other means of identification

Product number -
Other names 5-(3-METHOXY-PHENYL)-PENTA-2,4-DIENOIC 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:6500-63-6 SDS

6500-63-6Relevant articles and documents

The total synthesis of hypodematine

Kang, Zhi-Yun,Zhang, Qing-Jian,Chen, Ruo-Yun,Zhang, Pei-Cheng,Yu, De-Quan

, p. 840 - 848 (2013/09/23)

Hypodematine, isolated from Hypodematium sinense Iwatsuki as an alkaloid with a new skeleton, was synthesized via nine reaction steps, in which the synthesis of 2-aryl-1-benzazocines via Beckmann rearrangement of 5H-benzocyclohepten-5-one oxime mesylate i

Studies in Antifertility Agents: Part XXXIII- Synthesis of 1,2-trans-1--2-benzyl-7-methoxybenzosuberan

Sangwan, Naresh K.,Rastogi, Shri Nivas

, p. 140 - 143 (2007/10/02)

Condensation of 7-methoxy-1-benzosuberone (4) with PhCHO gives 2-benzylidene derivative (5) which on hydrogenation over Pd-C affords the corresponding 2-benzyl analog (6).Reduction of 6 with KBH4 furnishes a mixture of 1,2-cis- and trans-2-benzyl-1-benzos

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