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62008-36-0

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62008-36-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62008-36-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,0,0 and 8 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 62008-36:
(7*6)+(6*2)+(5*0)+(4*0)+(3*8)+(2*3)+(1*6)=90
90 % 10 = 0
So 62008-36-0 is a valid CAS Registry Number.
InChI:InChI=1/C50H77NO18/c1-29-19-17-15-13-11-9-7-8-10-12-14-16-18-20-37(68-49-47(62)44(51-33(5)52)46(61)32(4)67-49)26-41-43(48(63)65-6)40(58)28-50(64,69-41)27-36(55)24-39(57)38(56)22-21-34(53)23-35(54)25-42(59)66-31(3)30(2)45(29)60/h7-20,29-32,34-41,43-47,49,53-58,60-62,64H,21-28H2,1-6H3,(H,51,52)/b8-7+,11-9+,12-10-,15-13+,16-14+,19-17+,20-18+

62008-36-0SDS

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 methyl (4E,6E,8E,10E,12E,14E,16E)-3-(4-acetamido-3,5-dihydroxy-6-methyloxan-2-yl)oxy-19,25,27,30,31,33,35,37-octahydroxy-18,20,21-trimethyl-23-oxo-22,39-dioxabicyclo[33.3.1]nonatriaconta-4,6,8,10,12,14,16-heptaene-38-carboxylate

1.2 Other means of identification

Product number -
Other names Amphotericin B,N-acetyl-,methyl ester

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:62008-36-0 SDS

62008-36-0Downstream Products

62008-36-0Relevant articles and documents

Retrosynthetic and Synthetic Chemistry on Amphotericin B. Synthesis of C(1)-C(20) and C(21)-C(38) Fragments and Construction of the 38-Membered Macrocycle

Nicolaou, K. C.,Chakraborty, T. K.,Daines, R. A.,Simpkins, N. S.

, p. 413 - 416 (2007/10/02)

For the first time, amphotericin B (I) has been successfully derivatized and degraded to intermediates that have been converted into compounds (II) and (III) , projected as major key intermediates for a total synthesis; methods have been developed for the coupling of fragments (II) and (III) to give the ketophosphonate-aldehyde (28) and for the cyclization of this precursor to the 38-membered macrocyclic heptaenone (29) in 70-80percent yield.

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