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381230-85-9

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381230-85-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 381230-85-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,1,2,3 and 0 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 381230-85:
(8*3)+(7*8)+(6*1)+(5*2)+(4*3)+(3*0)+(2*8)+(1*5)=129
129 % 10 = 9
So 381230-85-9 is a valid CAS Registry Number.

381230-85-9SDS

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 N,N-dimethyl 5-oxopentanamide

1.2 Other means of identification

Product number -
Other names 5-Oxo-pentanoic acid dimethylamide

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:381230-85-9 SDS

381230-85-9Downstream Products

381230-85-9Relevant articles and documents

CATIONIC LIPID COMPOUNDS AND COMPOSITIONS THEREOF FOR USE IN THE DELIVERY OF MESSENGER RNA

-

, (2020/06/10)

The compounds disclosed herein compound of Formula (I), substructures thereof, and pharmaceutically acceptable salts thereof. The compounds provided herein can be useful for delivery and expression of mRNA and encoded protein, e.g., as a component of liposomal delivery vehicle, and accordingly can be useful for treating various diseases, disorders and conditions, such as those associated with deficiency of one or more proteins.

A Trialkylstannane-Mediated Approach to Acyloin Products

McGarvey, Glenn J.,Kimura, Masayuki

, p. 4655 - 4657 (2007/10/02)

α-Alkoxy organolithium compounds, generated through the treatment of the corresponding tri-n-butylstannane with n-BuLi, smoothly condense with N,N-dimethylamides to afford α-alkoxy carbonyl products.This condensation is functionally equivalent to a regiocontrolled acyloin condensation.

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