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328956-56-5

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328956-56-5 Usage

General Description

1-(2-BOC-AMINO-PHENYL)-ETHANOL is a chemical compound with the molecular formula C16H22N2O4. It is a white to off-white solid with a molecular weight of 302.35 g/mol. The compound contains a BOC-protected amino group and a hydroxyl group, making it a versatile intermediate in organic synthesis. It is commonly used as a building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. The BOC group can be easily removed under mild conditions, making 1-(2-BOC-AMINO-PHENYL)-ETHANOL a valuable precursor for the preparation of a wide range of functionalized compounds. Its properties and versatility make it a valuable tool in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 328956-56-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,8,9,5 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 328956-56:
(8*3)+(7*2)+(6*8)+(5*9)+(4*5)+(3*6)+(2*5)+(1*6)=185
185 % 10 = 5
So 328956-56-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H19NO3/c1-9(15)10-7-5-6-8-11(10)14-12(16)17-13(2,3)4/h5-9,15H,1-4H3,(H,14,16)

328956-56-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl N-[2-(1-hydroxyethyl)phenyl]carbamate

1.2 Other means of identification

Product number -
Other names GL-0164

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:328956-56-5 SDS

328956-56-5Relevant articles and documents

N-Heterocyclic Carbene-Catalyzed Synthesis of 2-Aryl Indoles

-

Paragraph 0065, (2015/11/27)

Transition metal-free catalytic methods for access to 2-arylindole compounds.

Enzymatic kinetic resolution of tert-butyl 2-(1-Hydroxyethyl) phenylcarbamate, a key intermediate to chiral organoselenanes and organotelluranes

Piovan, Leandro,Pasquini, Monica D.,Andrade, Leandro H.

experimental part, p. 8098 - 8109 (2011/11/06)

The enzymatic kinetic resolution of tert-butyl 2-(1-hydroxyethyl) phenylcarbamate via lipase-catalyzed transesterification reaction was studied. We investigated several reaction conditions and the carbamate was resolved by Candida antarctica lipase B (CAL

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