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85-17-6

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85-17-6 Usage

Definition

ChEBI: An amino cyclitol that is scyllo-inositol in which the hydroxy groups at positions 1 and 3 are replaced by guanidino groups.

Check Digit Verification of cas no

The CAS Registry Mumber 85-17-6 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 8 and 5 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 85-17:
(4*8)+(3*5)+(2*1)+(1*7)=56
56 % 10 = 6
So 85-17-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H18N6O4/c9-7(10)13-1-3(15)2(14-8(11)12)5(17)6(18)4(1)16/h1-6,15-18H,(H4,9,10,13)(H4,11,12,14)/t1-,2+,3?,4+,5-,6?

85-17-6SDS

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 streptidine

1.2 Other means of identification

Product number -
Other names 1,1'-(2,4,5,6-Tetrahydroxy-1,3-cyclohexylene)diguanidine

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:85-17-6 SDS

85-17-6Downstream Products

85-17-6Relevant articles and documents

Rescue of the streptomycin antibiotic activity by using streptidine as a "decoy acceptor" for the aminoglycoside-inactivating enzyme adenyl transferase

Latorre, Montserrat,Penalver, Pablo,Revuelta, Julia,Asensio, Juan Luis,Garcia-Junceda, Eduardo,Bastida, Agatha

, p. 2829 - 2831 (2007)

The use of streptidine as a "decoy acceptor" allows the antibiotic activity of streptomycin to recover against the Escherichia coli strain overexpressing the aminoglycoside-modifying enzyme 6-O-adenyl transferase. The Royal Society of Chemistry.

-

Peck et al.

, p. 29 (1946)

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