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38825-85-3

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38825-85-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38825-85-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,8,2 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 38825-85:
(7*3)+(6*8)+(5*8)+(4*2)+(3*5)+(2*8)+(1*5)=153
153 % 10 = 3
So 38825-85-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H15NO/c1-2-4-7-5-3-6-8/h7-8H,2-6H2,1H3

38825-85-3SDS

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-(propylamino)propan-1-ol

1.2 Other means of identification

Product number -
Other names AB4057

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:38825-85-3 SDS

38825-85-3Relevant articles and documents

Chen,Casida

, p. 263,264 (1978)

Benzazepine Dicarboxamide Compounds

-

Paragraph 0394; 0395; 0396, (2016/09/26)

This invention relates to novel benzazepine dicarboxamide compounds of the formula wherein R1 to R4 are as defined in the description and in the claims, as well as pharmaceutically acceptable salts thereof. These compounds are TLR agonists and may therefore be useful as medicaments for the treatment of diseases such as cancer, autoimmune diseases, inflammation, sepsis, allergy, asthma, graft rejection, graft-versus-host disease, immunodeficiencies, and infectious diseases.

Formation of 3-hydroxyalkyl carbamates from carbon dioxide, amines and oxetanes

Ishii, Shigeru,Zhou, Ming,Yoshida, Yasuhiko,Noguchi, Hiromichi

, p. 3207 - 3214 (2007/10/03)

The reactions of carbon dioxide, primary or secondary aliphatic amines and oxetanes at a CO2 pressure of 40 atm at 100-120°C without any catalysts afforded new monocarbamates of 1,3-propanediols, with concomitant formation of amino alcohols from oxetanes and amines.

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