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316155-84-7

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316155-84-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 316155-84-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,6,1,5 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 316155-84:
(8*3)+(7*1)+(6*6)+(5*1)+(4*5)+(3*5)+(2*8)+(1*4)=127
127 % 10 = 7
So 316155-84-7 is a valid CAS Registry Number.

316155-84-7SDS

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-ethenylpyridin-3-ol

1.2 Other means of identification

Product number -
Other names 3-hydroxy-2-vinylpyridine

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:316155-84-7 SDS

316155-84-7Downstream Products

316155-84-7Relevant articles and documents

New and efficient RCM in pyridinic series: synthesis of 2H-dihydropyrano- or 2,3H-dihydrooxepino[3,2-b]pyridines

Banaszak, Estelle,Comoy, Corinne,Fort, Yves

, p. 6235 - 6238 (2006)

A new and very efficient route to polycyclic heterocycles with isosteric replacement of benzene by pyridine is reported. This strategy involving the RCM reaction in pyridinic series as a keystep allows us to prepare 2H-dihydropyrano- or 2,3H-dihydrooxepino[3,2-b]pyridines 1 and 2 in very good overall yields (47% and 44%, respectively).

Furopyridines. XXXI [1]. Birch reduction of furopyridines

Yamaguchi, Seiji,Hamade, Eriko,Yokoyama, Hajime,Hirai, Yoshiro,Shiotani, Shunsaku

, p. 335 - 339 (2007/10/03)

Birch reduction of four furopyridines 1a-d effected the characteristic cleavage of the furan ring, giving ethnylpyridinols 2a-d, vinylpyridinols 3b,d, and ethylpyridinols 4a-d, and the reduction of the furan ring, giving dihydrofuropyridine 5c,d.

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