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2625-41-4

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2625-41-4 Usage

Synthesis Reference(s)

Synthesis, p. 826, 1986 DOI: 10.1055/s-1986-31791

Check Digit Verification of cas no

The CAS Registry Mumber 2625-41-4 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, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2625-41:
(6*2)+(5*6)+(4*2)+(3*5)+(2*4)+(1*1)=74
74 % 10 = 4
So 2625-41-4 is a valid CAS Registry Number.
InChI:InChI=1/C4H7NO2/c6-5(7)4-2-1-3-4/h4H,1-3H2

2625-41-4SDS

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 nitrocyclobutane

1.2 Other means of identification

Product number -
Other names nitro-cyclobutane

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:2625-41-4 SDS

2625-41-4Relevant articles and documents

INHIBITORS OF NOROVIRUS AND CORONAVIRUS REPLICATION

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Paragraph 002054-002056, (2021/10/15)

Compounds of Formula (I) and methods of inhibiting the replication of viruses in a biological sample or patient, of reducing the amount of viruses in a biological sample or patient, and of treating a virus infection in a patient, comprising administering to said biological sample or patient an effective amount of a compound represented by Formula (I), a compound of Table A or B or a pharmaceutically acceptable salt thereof.

Direct and Efficient Preparation of gem-Chloronitro Compounds or Nitro Compounds from gem-Bromonitro Compounds

Amrollah-Madjdabadi, A.,Beugelmans, R.,Lechevallier, A.

, p. 826 - 828 (2007/10/02)

Sodiumethanethiolate in methanol is an efficient reducing agent for gem-bromonitro compounds; treatment of the resultant nitronates with a protic acid or with N-chlorosuccinimide gives high yields of the corresponding nitro or gem-chloronitro compounds, respectively.

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