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16400-13-8

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16400-13-8 Usage

Uses

7-Methyl-4-indanol is used as an intermediate in synthetic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 16400-13-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,4,0 and 0 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 16400-13:
(7*1)+(6*6)+(5*4)+(4*0)+(3*0)+(2*1)+(1*3)=68
68 % 10 = 8
So 16400-13-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O/c1-7-5-6-10(11)9-4-2-3-8(7)9/h5-6,11H,2-4H2,1H3

16400-13-8 Well-known Company Product Price

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  • Alfa Aesar

  • (B20343)  7-Methyl-4-indanol, 97%   

  • 16400-13-8

  • 2.5g

  • 883.0CNY

  • Detail
  • Alfa Aesar

  • (B20343)  7-Methyl-4-indanol, 97%   

  • 16400-13-8

  • 10g

  • 2516.0CNY

  • Detail

16400-13-8SDS

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 7-methyl-2,3-dihydro-1H-inden-4-ol

1.2 Other means of identification

Product number -
Other names 7-Methylindan-4-ol

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:16400-13-8 SDS

16400-13-8Relevant articles and documents

Synthesis of substituted benzenes and phenols by ring-closing olefin metathesis

Yoshida, Kazuhiro,Takahashi, Hidetoshi,Imamoto, Tsuneo

experimental part, p. 8246 - 8261 (2009/09/29)

New synthetic approaches to substituted aromatic compounds are reported. Ring-closing olefin metathesis (RCM)/dehydration and RCM/tautomerization are the key processes in the synthesis of substituted benzenes 3 and phenols 6, respectively. Readily accessible 1,5,7-trien-4-ols 7, which are the precursors of benzenes, were prepared from β-halo-α, β-unsaturated aldehydes 11 or β-halo-α,β-unsaturated esters 19 by utilizing reliable transformations in which cross-coupling with vinylic metal reagents 12 and allylation with allylic metal reagents 13 were employed as carbon-carbon bond forming reactions. RCM of 7, followed by dehydration, afforded a wide variety of substituted benzenes 3. In addition, RCM of 1,5,7trien-4-ones 9, which were prepared by oxidation of 7, furnished various substituted phenols 6 by automatic tautomerization.

The Generation of 2-Vinylcyclopentene-1,3-diones via a Five-Component Coupling in the Coordination Sphere of Chromium

Xu, Yao-Chang,Challener, Cynthia A.,Dragisich, Vera,Brandvold, Timothy A.,Peterson, Glen A.,et al.

, p. 7269 - 7271 (2007/10/02)

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