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94135-98-5

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94135-98-5 Usage

Physical state

Colorless to yellowish liquid

Odor

Strong, sweet, and pleasant

Natural occurrence

Found in essential oils such as sassafras oil and camphor oil

Industrial use

Precursor in the synthesis of illegal drug MDMA (ecstasy)

Regulatory status

Banned as a food additive in the United States due to potential carcinogenic properties

International use

Used as a flavoring agent in some countries

Additional applications

Precursor for the synthesis of various perfumes and pesticides

Check Digit Verification of cas no

The CAS Registry Mumber 94135-98-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,1,3 and 5 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 94135-98:
(7*9)+(6*4)+(5*1)+(4*3)+(3*5)+(2*9)+(1*8)=145
145 % 10 = 5
So 94135-98-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H12O4/c12-10(13)6-2-4-8-3-1-5-9-11(8)15-7-14-9/h1,3,5H,2,4,6-7H2,(H,12,13)

94135-98-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(1,3-benzodioxol-4-yl)butanoic acid

1.2 Other means of identification

Product number -
Other names 4-[(2,3-methylenedioxy)phenyl]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:94135-98-5 SDS

94135-98-5Upstream product

94135-98-5Relevant articles and documents

Synthesis of 1-tetralone derivatives using a Stille cross coupling/friedel crafts acylation sequence

Vercouillie, Johnny,Abarbri, Mohamed,Parrain, Jean-Luc,Duchene, Alain,Thibonnet, Jerome

, p. 3751 - 3762 (2007/10/03)

An efficient method of synthesis of 1-tetralones has been achieved featuring a Stille cross-coupling reaction as the key step.

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