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76888-68-1

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76888-68-1 Usage

General Description

3-(Ethylamino)butan-1-ol is a chemical compound with the molecular formula C6H15NO. It belongs to the class of organic compounds known as amino alcohols, specifically, secondary amino alcohols. These are organic compounds containing an alkyl chain with an amino group and at least one alcohol group. The ethylamino group indicates the presence of an ethyl group attached to the nitrogen atom. It has one alcohol (OH) functional group attached to its first carbon atom, which is indicated by the suffix 'ol' in the name. This chemical is typically used in the synthesis of other compounds in chemical reactions, particularly in the pharmaceutical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 76888-68-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,8,8 and 8 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 76888-68:
(7*7)+(6*6)+(5*8)+(4*8)+(3*8)+(2*6)+(1*8)=201
201 % 10 = 1
So 76888-68-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H15NO/c1-3-7-6(2)4-5-8/h6-8H,3-5H2,1-2H3

76888-68-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(Ethylamino)butan-1-ol

1.2 Other means of identification

Product number -
Other names 1-Butanol,3-(ethylamino)

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:76888-68-1 SDS

76888-68-1Downstream Products

76888-68-1Relevant articles and documents

Enantioselective synthesis of β-amino acids based on BINAP-ruthenium(II) catalyzed hydrogenation

Lubell,Kitamura,Noyori

, p. 543 - 554 (2007/10/02)

BINAP-Ru(II) catalyzed hydrogenation of β-substituted (E)-β-(acylamino)acrylic acids allows efficient enantioselective synthesis of β-amino acids. The Z double bond isomers which possess an intramolecular hydrogen bond between amide and ester groups are more reactive but are hydrogenated with poor enantioselectivity. BINAP-Rh(I) complexes afford only moderate stereoselectivity with the opposite sense of enantioselection.

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