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16563-48-7

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16563-48-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16563-48-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,5,6 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 16563-48:
(7*1)+(6*6)+(5*5)+(4*6)+(3*3)+(2*4)+(1*8)=117
117 % 10 = 7
So 16563-48-7 is a valid CAS Registry Number.

16563-48-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2-naphthoxy)-butanoic acid

1.2 Other means of identification

Product number -
Other names 4-(2-naphthoxy)butanoic 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:16563-48-7 SDS

16563-48-7Downstream Products

16563-48-7Relevant articles and documents

Potential hypotensive agents: Synthesis and hypotensive activity of oxime ethers derived from 1-naphthoxepines and related compounds

Tandon, Vishnu K.,Kumar, Manoj,Awasthi, Anoop K.,Saxena, Hari O.,Goswamy, Gajendra K.

, p. 3177 - 3180 (2007/10/03)

The synthesis and pharmacological evaluation of substituted oximino-ethers 1 and 2 of naphth[1,2-b]- and naphth[2,1-b]-oxepin-5-ones (4 and 8) were carried out. The hypotensive activity of oximino-ethers 1 and 2 was evaluated on anaesthetized cats. The results indicated that 1c caused a fall of 80mm/Hg for >100′ at a dose of 5mg/kg iv in anaesthetized cats.

An improved two-step regioselective synthesis of naphth- and naphthoxepin-5-ones

Tandon, V. K.,Chhor, R. B.,Goswamy, G. K.

, p. 1027 - 1029 (2007/10/03)

An improved regioselective synthesis of naphthoxepin-5-one 1 and naphthoxepin-5-one 2 has been described. The key step is one-step regioselective synthesis of 4-naphthoxybutanoic acids 3 and 4, formed from the corresponding naphthols, and their cyclisation to naphthoxepinones 1 and 2.

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