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954-54-1

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954-54-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 954-54-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,5 and 4 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 954-54:
(5*9)+(4*5)+(3*4)+(2*5)+(1*4)=91
91 % 10 = 1
So 954-54-1 is a valid CAS Registry Number.

954-54-1SDS

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 3,4-diphenylfuran

1.2 Other means of identification

Product number -
Other names Furan,3,4-diphenyl

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:954-54-1 SDS

954-54-1Relevant articles and documents

Photochemistry of thiophene-S-oxide derivatives

Heying, Melanie J.,Nag, Mrinmoy,Jenks, William S.

experimental part, p. 915 - 924 (2009/10/26)

Photolysis of substituted thiophene-S-oxides in solution results in the formation of either the corresponding thiophene or furan, in addition to uncharacterized materials. No good rationalization is available for the choice of which pathway may predominat

Magnesium mediated carbometallation of propargyl alcohols: Direct routes to furans and furanones

Forgione, Pat,Wilson, Peter D.,Fallis, Alex G.

, p. 17 - 20 (2007/10/03)

The addition of vinyl and aryl Grignard reagents to propargyl alcohols for the direct synthesis of furans and butenolides from a one pot reaction is described. These products arise from a putative magnesium chelate intermediate 2 upon reaction with various electrophiles. This chelate was also generated in situ from alkynyl lithium addition to aldehydes followed by magnesium exchange and Grignard addition. Thus, the complete substitution pattern for the furan ring may be controlled, as desired, through the judicious choice of substrates and reagents.

3,4-Bis(tributylstannyl)furan: a Versatile Building Block for the Regiospecific Synthesis of 3,4-Disubstituted Furans

Yang, Yun,Wong, Henry N. C.

, p. 656 - 658 (2007/10/02)

By utilising an oxazole-alkyne Diels-Alder reaction, 3,4-bis(tributylstannyl)furan is prepared and its synthetic potential assessed by its conversion into several 3,4-disubstituted furans via Stille-type palladium-catalysed reactions.

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