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3-(Ethylamino)butan-1-ol is a chemical compound with the molecular formula C6H15NO, belonging to the class of organic compounds known as secondary amino alcohols. These compounds are characterized by an alkyl chain with an amino group and at least one alcohol group. The ethylamino group in its structure signifies the presence of an ethyl group attached to the nitrogen atom, while the alcohol (OH) functional group is attached to its first carbon atom, as indicated by the suffix 'ol' in the name.

76888-68-1

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76888-68-1 Usage

Uses

Used in Pharmaceutical Industry:
3-(Ethylamino)butan-1-ol is used as a synthetic intermediate for the production of various pharmaceutical compounds. Its unique structure allows it to be a versatile building block in the synthesis of drugs, contributing to the development of new medications.
Used in Chemical Reactions:
3-(Ethylamino)butan-1-ol is used as a reagent in various chemical reactions, particularly in the synthesis of other organic compounds. Its presence in these reactions can facilitate the formation of desired products, making it a valuable component in the field of organic chemistry.

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 academic research and scientific papers

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.

The Conformational Analysis of Saturated Heterocycles. Part 100. 1-Oxa-3-azacyclohexanes

Katritzky, Alan R.,Baker, Victor J.,Brito-Palma, Fernando M. S.

, p. 1739 - 1745 (2007/10/02)

Conformational equilibria and barriers to ring and nitrogen inversion are determined by 1H and 13C n.m.r. for 13 1-oxa-3-azacyclohexanes and correlated with recent work on the conformational analysis of saturated heterocycles.

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