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benzyl [3-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)propyl]carbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17415-87-1

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17415-87-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17415-87-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,4,1 and 5 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 17415-87:
(7*1)+(6*7)+(5*4)+(4*1)+(3*5)+(2*8)+(1*7)=111
111 % 10 = 1
So 17415-87-1 is a valid CAS Registry Number.

17415-87-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Phthalimido-N-benzyloxycarbonylpropylamin

1.2 Other means of identification

Product number -
Other names 3-phthalimidomethyl-3-methyloxetane

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:17415-87-1 SDS

17415-87-1Relevant academic research and scientific papers

A novel, one-step method for the conversion of primary alcohols into carbamate-protected amines

Wood, Michael R.,Kim, June Y.,Books, Kathy M.

, p. 3887 - 3890 (2007/10/03)

A novel process for the one-step conversion of primary alcohols into carbamate-protected amines has been developed using a modified Burgess reagent. Although this letter mainly focuses on the conversion of alcohols into the corresponding Cbz-protected amines, the potential for extending this process to a wide range of carbamates has also been demonstrated. A detailed catalytic cycle has been proposed. While exploring the scope of this new reagent, an N-aryl piperidine to an N-aryl pyrrolidine rearrangement has been observed and rationalized.

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