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476615-02-8

2-Buten-1-ol,3-methyl-,4-aminobenzoate(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

476615-02-8

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476615-02-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 476615-02-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,6,6,1 and 5 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 476615-02:
(8*4)+(7*7)+(6*6)+(5*6)+(4*1)+(3*5)+(2*0)+(1*2)=168
168 % 10 = 8
So 476615-02-8 is a valid CAS Registry Number.

476615-02-8SDS

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-methylbut-2-enyl 4-aminobenzoate

1.2 Other means of identification

Product number -
Other names -

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:476615-02-8 SDS

476615-02-8Downstream Products

476615-02-8Relevant articles and documents

Palladium-catalyzed silane/siloxane reductions in the one-pot conversion of nitro compounds into their amines, hydroxylamines, amides, sulfonamides, and carbamates

Rahaim Jr., Ronald J.,Maleczka Jr., Robert E.

, p. 3316 - 3340 (2008/09/17)

A combination of palladium(II) acetate, aqueous potassium fluoride, and polymethylhydrosiloxane (PMHS) facilitates the room-temperature reduction of aromatic nitro compounds to anilines. These reactions tend to be quick (30 min), high-yielding, and tolerate a range of other functional groups. Replacement of PMHS/KF with triethylsilane allows for the reduction of aliphatic nitro compounds to their corresponding hydroxylamines. Depending on the substrate, both conditions can allow for the in situ conversion of the product amines into amides, sulfonamides, and carbamates. Georg Thieme Verlag Stuttgart.

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