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2625-37-8

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2625-37-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2625-37-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,2 and 5 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2625-37:
(6*2)+(5*6)+(4*2)+(3*5)+(2*3)+(1*7)=78
78 % 10 = 8
So 2625-37-8 is a valid CAS Registry Number.

2625-37-8SDS

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 4-nitroheptane

1.2 Other means of identification

Product number -
Other names 4-nitro-heptane

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:2625-37-8 SDS

2625-37-8Relevant articles and documents

Facile access to nitroalkanes: Nitration of alkanes by selective C[sbnd]H nitration using metal nitrate, catalyzed by in-situ generated metal oxide

Li, Na,Mao, Liqiu,Peng, Haoyu,Peng, Ling,Yin, Dulin,You, Kuiyi,Zhong, Wenzhou

, (2020/05/13)

Direct C ? H functionalization of inactive alkanes is an important strategy to streamline the preparation of functional molecules. Herein, we describe an operationally simple and effective alkane C ? H nitration reaction to access versatile nitroalkanes without cleavage of the C ? C skeleton. Nontoxic and inexpensive metal nitrate (Fe(NO3)3·9H2O) plays a dual role as catalyst precursors as well as nitro sources for the transformation. Experimental evidence and theoretical modeling have shown the formation of iron oxide as a key catalytic species for the alkane C ? H and NO2 activation, which favors a stepwise radical mechanism with initial alkyl radical formation.

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