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54774-89-9

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54774-89-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54774-89-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,7,7 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 54774-89:
(7*5)+(6*4)+(5*7)+(4*7)+(3*4)+(2*8)+(1*9)=159
159 % 10 = 9
So 54774-89-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H16/c1-3-6-13-11(2)9-10-12-7-4-5-8-14(12)13/h4-5,7-10H,3,6H2,1-2H3

54774-89-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-1-propylnaphthalene

1.2 Other means of identification

Product number -
Other names Naphthalene, 2-methyl-1-propyl-

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:54774-89-9 SDS

54774-89-9Upstream product

54774-89-9Downstream Products

54774-89-9Relevant articles and documents

Efficient cross-coupling of aryl/alkenyl triflates with acyclic secondary alkylboronic acids

Si, Tengda,Li, Bowen,Xiong, Wenrui,Xu, Bin,Tang, Wenjun

supporting information, p. 9903 - 9909 (2017/12/12)

Aryl-secondary alkyl cross-coupling with aryl sulfonate esters as coupling partners remains a significant challenge. Efficient cross-coupling between aryl/alkenyl triflates and acyclic secondary alkylboronic acids is realized for the first time to provide a series of sterically congested acyclic secondary alkyl arenes/olefins in good to excellent yields. The employment of sterically bulky P,PO ligand L1/L2 is crucial for the high yields and selectivities. The method has enabled a concise and 4-step synthesis of a key intermediate of male contraceptive agent and PAF antagonist gossypol.

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