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N-[(5-hydroxypentyl)carbamoyl]-3-methoxy-2-methylprop-2-enamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

78795-17-2

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78795-17-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78795-17-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,7,9 and 5 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 78795-17:
(7*7)+(6*8)+(5*7)+(4*9)+(3*5)+(2*1)+(1*7)=192
192 % 10 = 2
So 78795-17-2 is a valid CAS Registry Number.

78795-17-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(5-hydroxypentylcarbamoyl)-3-methoxy-2-methylprop-2-enamide

1.2 Other means of identification

Product number -
Other names -

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:78795-17-2 SDS

78795-17-2Downstream Products

78795-17-2Relevant academic research and scientific papers

Carbocyclic Analogs of Thymine Nucleosides and Related 1-Substituted Thymines

Shealy, Y.Fulmer,O'Dell, C.Allen,Thorpe, Martha C.

, p. 383 - 389 (2007/10/02)

The carbocyclic analogs of thymidine (IXf), 1-β-ribofuranosylthymine (IXg), and 1-β-3'-deoxyribofuranosylthymine (IXe) were synthesized by incorporating modifications into the Shaw method of synthesizing 2,4-(1H,3H)pyrimidinediones via acryloylureas.Simpler analogs of thymine nucleosides were also prepared by this method.The carbocyclic analog of thymidine displayed modest activity against Leukemia L1210 in vivo.It differs from a compound prepared previously by a Prins reaction.

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