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7668-55-5

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7668-55-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7668-55-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,6 and 8 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7668-55:
(6*7)+(5*6)+(4*6)+(3*8)+(2*5)+(1*5)=135
135 % 10 = 5
So 7668-55-5 is a valid CAS Registry Number.

7668-55-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R)-2-naphthalen-2-yloxybutanoic acid

1.2 Other means of identification

Product number -
Other names Butanoic acid,2-(2-naphthalenyloxy)-,(R)

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:7668-55-5 SDS

7668-55-5Upstream product

7668-55-5Downstream Products

7668-55-5Relevant articles and documents

Asymmetric hydrogenation of α,β-unsaturated carboxylic acids catalyzed by ruthenium(II) complexes of spirobifluorene diphosphine (SFDP) ligands

Cheng, Xu,Xie, Jian-Hua,Li, Sheng,Zhou, Qi-Lin

, p. 1271 - 1276 (2006)

The ruthenium diacetate complexes ligated by chiral spirobifluorene diphosphines (SFDP) were very effective catalysts for the asymmetric hydrogenation of tiglic acid derivatives and α-methylcinnamic acid derivatives with high activities and excellent enantioselectivities (up to 98% ee). The α-aryloxybutenoic acids can also be hydrogenated by these catalysts to provide the corresponding saturated α-aryloxybutanoic acids in high yields (89-93%) and enantioselectivities (up to 95% ee). In this reaction, the SFDP ligand with para-methyl groups on the P-phenyl rings gave the best results.

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